A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545113



Internal ID18843394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:43096276..43107032hg38UCSC Ensembl
Innerchr17:41248293..41259049hg19UCSC Ensembl
Innerchr17:38501819..38512575hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3810757
hg1910757
hg1810757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058376
Supporting Variants
Samples
Known GenesBRCA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3545113
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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