A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623823



Internal ID7010679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74139436..74141271hg38UCSC Ensembl
Innerchr10:74139465..74141242hg38UCSC Ensembl
Outerchr10:74139407..74141300hg38UCSC Ensembl
chr10:75899194..75901029hg19UCSC Ensembl
Innerchr10:75899223..75901000hg19UCSC Ensembl
Outerchr10:75899165..75901058hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381836
hg191836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13863607, essv13863610, essv13863614, essv13863609, essv13863611, essv13863616, essv13863608, essv13863615, essv13863612, essv13863613
SamplesHG02272, HG02105, HG01277, NA19649, HG02104, NA19031, NA19740, HG02455, NA19735, NA19741
Known GenesAP3M1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623823
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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