A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560908



Internal ID18512503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20255030..20353185hg38UCSC Ensembl
Innerchr17:20158343..20256498hg19UCSC Ensembl
Innerchr17:20098935..20197090hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3898156
hg1998156
hg1898156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057389
Supporting Variants
Samples
Known GenesCCDC144CP, SPECC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560908
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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