A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3561062



Internal ID18859343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33342525..33368756hg38UCSC Ensembl
Innerchr17:31669543..31695774hg19UCSC Ensembl
Innerchr17:28693656..28719887hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3826232
hg1926232
hg1826232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058478
Supporting Variants
Samples
Known GenesASIC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3561062
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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