A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3561059



Internal ID18859340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33330590..33353893hg38UCSC Ensembl
Innerchr17:31657608..31680911hg19UCSC Ensembl
Innerchr17:28681721..28705024hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3823304
hg1923304
hg1823304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065524
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)nssv3561059
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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