A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622141



Internal ID6662311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2646620..3092104hg38UCSC Ensembl
Innerchr10:2646770..3091954hg38UCSC Ensembl
Outerchr10:2646470..3092254hg38UCSC Ensembl
chr10:2688812..3134296hg19UCSC Ensembl
Innerchr10:2688962..3134146hg19UCSC Ensembl
Outerchr10:2688662..3134446hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38445485
hg19445485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13673340, essv13673331, essv13673335, essv13673330, essv13673329, essv13673333, essv13673336, essv13673332, essv13673337, essv13673339, essv13673338, essv13673334
SamplesHG03559, HG03521, HG02536, HG03372, NA18510, NA19374, HG03086, NA19201, HG03267, HG00533, NA19147, HG01886
Known GenesPFKP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622141
Frequency
Sample Size2504
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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