A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559596



Internal ID18511191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75499761..75542099hg38UCSC Ensembl
Innerchr16:75533659..75575997hg19UCSC Ensembl
Innerchr16:74091160..74133498hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3842339
hg1942339
hg1842339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062535
Supporting Variants
Samples
Known GenesCHST5, TMEM231
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559596
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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