A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566099



Internal ID18864380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52881388..53237046hg38UCSC Ensembl
Innerchr17:50958748..51314407hg19UCSC Ensembl
Innerchr17:48313747..48669406hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38355659
hg19355660
hg18355660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062893
Supporting Variants
Samples
Known GenesC17orf112
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566099
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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