A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13765005



Internal ID917420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44535964..44537968hg38UCSC Ensembl
Innerchr10:44535964..44537968hg38UCSC Ensembl
Outerchr10:44535697..44538223hg38UCSC Ensembl
chr10:45031412..45033416hg19UCSC Ensembl
Innerchr10:45031412..45033416hg19UCSC Ensembl
Outerchr10:45031145..45033671hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382005
hg192005
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623064
Supporting Variants
SamplesHG00542
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13765005
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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