A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624260



Internal ID6664427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94768157..94807834hg38UCSC Ensembl
Innerchr10:94768169..94807823hg38UCSC Ensembl
Outerchr10:94768146..94807846hg38UCSC Ensembl
chr10:96527914..96567591hg19UCSC Ensembl
Innerchr10:96527926..96567580hg19UCSC Ensembl
Outerchr10:96527903..96567603hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3839678
hg1939678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13902097, essv13902096
SamplesHG01771, HG00268
Known GenesCYP2C19
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624260
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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