A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567729



Internal ID18519324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:65545060..65595509hg38UCSC Ensembl
Innerchr17:63541178..63591627hg19UCSC Ensembl
Innerchr17:60971640..61022089hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3850450
hg1950450
hg1850450
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058285
Supporting Variants
Samples
Known GenesAXIN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567729
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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