A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065921



Internal ID18808452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81415451..81457288hg38UCSC Ensembl
Innerchr17:79389251..79424314hg19UCSC Ensembl
Innerchr17:77003846..77038909hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3841838
hg1935064
hg1835064
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3293n100
Supporting Variantsnssv3567874, nssv3567873
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)nsv1065921
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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