A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560879



Internal ID18859160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19596411..19639849hg38UCSC Ensembl
Innerchr17:19499724..19543162hg19UCSC Ensembl
Innerchr17:19440316..19483754hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3843439
hg1943439
hg1843439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058288
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560879
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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