A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9893923



Internal ID6592794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26504833..26513567hg38UCSC Ensembl
Innerchr1:26504883..26513517hg38UCSC Ensembl
Outerchr1:26504781..26513619hg38UCSC Ensembl
chr1:26831324..26840058hg19UCSC Ensembl
Innerchr1:26831374..26840008hg19UCSC Ensembl
Outerchr1:26831272..26840110hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg388735
hg198735
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585541
Supporting Variants
SamplesNA20768
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9893923
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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