A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1062636



Internal ID15915822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65512086..65611651hg38UCSC Ensembl
Innerchr6:66221979..66321544hg19UCSC Ensembl
Innerchr6:66278700..66378265hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3899566
hg1999566
hg1899566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603442
Supporting Variants
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1062636
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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