A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8949926



Internal ID13217551
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 StatusS
Merged Variantsesv3321957
Supporting Variants
SamplesNA11920
Known GenesC10orf131, ENTPD1-AS1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8949926
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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