A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636367



Internal ID7023161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:46438084..46438885hg38UCSC Ensembl
Innerchr15:46438085..46438884hg38UCSC Ensembl
Outerchr15:46438083..46438886hg38UCSC Ensembl
chr15:46730282..46731083hg19UCSC Ensembl
Innerchr15:46730283..46731082hg19UCSC Ensembl
Outerchr15:46730281..46731084hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15238491, essv15238488, essv15238493, essv15238490, essv15238492, essv15238485, essv15238494, essv15238495, essv15238496, essv15238487, essv15238489, essv15238486
SamplesHG02870, HG02922, HG02634, HG02442, HG02570, HG02582, HG03391, HG02799, HG01912, HG02053, HG02679, HG02763
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636367
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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