A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654696



Internal ID18952977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:356103..384097hg38UCSC Ensembl
Innerchr6:356103..384097hg19UCSC Ensembl
Innerchr6:301103..329097hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3827995
hg1927995
hg1827995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016278
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)nssv3654696
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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