A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062535



Internal ID18805066
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 StatusM
Merged Variantsdgv3020n100
Supporting Variantsnssv3559591, nssv3559593, nssv3559596, nssv3559584, nssv3559590, nssv3559583, nssv3559585, nssv3559586, nssv3559589, nssv3559588, nssv3559587, nssv3559595, nssv3719034, nssv3559592, nssv3559594
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)nsv1062535
Frequency
Sample Size29084
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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