A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718891



Internal ID19017172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13792526..13842439hg38UCSC Ensembl
Innerchr16:13886383..13936296hg19UCSC Ensembl
Innerchr16:13793884..13843797hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3849914
hg1949914
hg1849914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053805
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)nssv3718891
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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