A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560433



Internal ID18858714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:18375163..18571320hg38UCSC Ensembl
Innerchr17:18278477..18474634hg19UCSC Ensembl
Innerchr17:18219202..18415359hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38196158
hg19196158
hg18196158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058895
Supporting Variants
Samples
Known GenesCCDC144B, EVPLL, FAM106A, FLJ35934, KRT16P1, LGALS9C, LOC339240, USP32P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560433
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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