A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062256



Internal ID18804787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81418559..81479952hg38UCSC Ensembl
Innerchr17:79392359..79446978hg19UCSC Ensembl
Innerchr17:77006954..77061573hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3861394
hg1954620
hg1854620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3295n100
Supporting Variantsnssv3567888, nssv3567887
Samples
Known GenesBAHCC1, MIR3186
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062256
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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