A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560911



Internal ID18859192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20389766..20530544hg38UCSC Ensembl
Innerchr17:20293079..20433857hg19UCSC Ensembl
Innerchr17:20233671..20374449hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38140779
hg19140779
hg18140779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055600
Supporting Variants
Samples
Known GenesCCDC144CP, KRT16P3, LGALS9B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560911
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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