A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622639



Internal ID7009497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24315634..24318044hg38UCSC Ensembl
Innerchr10:24315634..24318044hg38UCSC Ensembl
Outerchr10:24315320..24318357hg38UCSC Ensembl
chr10:24604563..24606973hg19UCSC Ensembl
Innerchr10:24604563..24606973hg19UCSC Ensembl
Outerchr10:24604249..24607286hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg382411
hg192411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13718782, essv13718781
SamplesHG00106, HG01171
Known GenesKIAA1217
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622639
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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