A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648865



Internal ID18947146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80875732..80911578hg38UCSC Ensembl
Innerchr6:81585449..81621295hg19UCSC Ensembl
Innerchr6:81642168..81678014hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3835847
hg1935847
hg1835847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022379
Supporting Variants
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)nssv3648865
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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