A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3321957



Internal ID15168931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95908770..95908782hg38UCSC Ensembl
Innerchr10:95908761..95908791hg38UCSC Ensembl
Outerchr10:95908747..95908803hg38UCSC Ensembl
chr10:97668527..97668539hg19UCSC Ensembl
Innerchr10:97668518..97668548hg19UCSC Ensembl
Outerchr10:97668504..97668560hg19UCSC Ensembl
chr10:97658517..97658529hg18UCSC Ensembl
Innerchr10:97658538..97658508hg18UCSC Ensembl
Outerchr10:97658494..97658550hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8949938, essv8949954, essv8949953, essv8949931, essv8949937, essv8949927, essv8949955, essv8949941, essv8949948, essv8949951, essv8949950, essv8949935, essv8949928, essv8949943, essv8949942, essv8949939, essv8949933, essv8949956, essv8949949, essv8949945, essv8949926, essv8949929, essv8949940, essv8949934, essv8949924, essv8949957, essv8949930, essv8949952, essv8949946, essv8949944, essv8949932
SamplesNA11830, NA11995, NA11920, NA18603, NA12045, NA12751, NA18870, NA18510, NA12750, NA07357, NA07346, NA11992, NA12287, NA19138, NA11994, NA10847, NA18951, NA12003, NA18573, NA11919, NA18856, NA12249, NA18555, NA12043, NA18542, NA18909, NA11881, NA18564, NA07037, NA18522, NA12154
Known GenesC10orf131, ENTPD1-AS1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3321957
Frequency
Sample Size185
Observed Gain31
Observed Loss0
Observed Complex0
Frequencyn/a


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