A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622575



Internal ID7009433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21320532..21321616hg38UCSC Ensembl
Innerchr10:21320532..21321616hg38UCSC Ensembl
Outerchr10:21320299..21321848hg38UCSC Ensembl
chr10:21609461..21610545hg19UCSC Ensembl
Innerchr10:21609461..21610545hg19UCSC Ensembl
Outerchr10:21609228..21610777hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381085
hg191085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13715206, essv13715205
SamplesHG00629, NA18624
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622575
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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