A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560889



Internal ID18859170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19596411..19640964hg38UCSC Ensembl
Innerchr17:19499724..19544277hg19UCSC Ensembl
Innerchr17:19440316..19484869hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3844554
hg1944554
hg1844554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064042
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)nssv3560889
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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