A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032687



Internal ID18775221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:133666234..133738590hg38UCSC Ensembl
Innerchr6:133987372..134059728hg19UCSC Ensembl
Innerchr6:134029065..134101421hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3872357
hg1972357
hg1872357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6148n100
Supporting Variantsnssv3654398
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032687
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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