A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657502



Internal ID18955783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:56786447..56835651hg38UCSC Ensembl
Innerchr6:56651245..56700449hg19UCSC Ensembl
Innerchr6:56759204..56808408hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3849205
hg1949205
hg1849205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034418
Supporting Variants
Samples
Known GenesDST
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657502
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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