A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13756427



Internal ID6852887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36360120..36361776hg38UCSC Ensembl
Innerchr10:36360155..36361742hg38UCSC Ensembl
Outerchr10:36360086..36361811hg38UCSC Ensembl
chr10:36649048..36650704hg19UCSC Ensembl
Innerchr10:36649083..36650670hg19UCSC Ensembl
Outerchr10:36649014..36650739hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381657
hg191657
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622921
Supporting Variants
SamplesNA21088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13756427
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer