A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9863651



Internal ID6488944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15594076..15610996hg38UCSC Ensembl
Innerchr1:15594576..15610496hg38UCSC Ensembl
Outerchr1:15593076..15611996hg38UCSC Ensembl
chr1:15920571..15937491hg19UCSC Ensembl
Innerchr1:15921071..15936991hg19UCSC Ensembl
Outerchr1:15919571..15938491hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3816921
hg1916921
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585313
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9863651
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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