A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560582



Internal ID18858863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19594577..19635122hg38UCSC Ensembl
Innerchr17:19497890..19538435hg19UCSC Ensembl
Innerchr17:19438482..19479027hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3840546
hg1940546
hg1840546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065299
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)nssv3560582
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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