A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13902097



Internal ID3903913
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624260
Supporting Variants
SamplesHG01771
Known GenesCYP2C19
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13902097
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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