A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10264977



Internal ID266793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201558582..201559507hg38UCSC Ensembl
Innerchr1:201558632..201559457hg38UCSC Ensembl
Outerchr1:201558532..201559557hg38UCSC Ensembl
chr1:201527710..201528635hg19UCSC Ensembl
Innerchr1:201527760..201528585hg19UCSC Ensembl
Outerchr1:201527660..201528685hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38926
hg19926
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3588572
Supporting Variants
SamplesHG03382
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10264977
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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