A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3303997



Internal ID15150945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95770456..95770457hg38UCSC Ensembl
Innerchr10:95770434..95770479hg38UCSC Ensembl
Outerchr10:95770433..95770480hg38UCSC Ensembl
chr10:97530213..97530214hg19UCSC Ensembl
Innerchr10:97530191..97530236hg19UCSC Ensembl
Outerchr10:97530190..97530237hg19UCSC Ensembl
chr10:97520203..97520204hg18UCSC Ensembl
Innerchr10:97520226..97520181hg18UCSC Ensembl
Outerchr10:97520180..97520227hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38292
hg19292
hg18292
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7764902
SamplesNA12812
Known GenesENTPD1, ENTPD1-AS1
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3303997
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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