A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3548604



Internal ID18500199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46110933..46190497hg38UCSC Ensembl
Innerchr17:44188299..44267863hg19UCSC Ensembl
Innerchr17:41544082..41623640hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3879565
hg1979565
hg1879559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055440
Supporting Variants
Samples
Known GenesKANSL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3548604
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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