A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3723889



Internal ID18675484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46136346..46588293hg38UCSC Ensembl
Innerchr17:44213712..44665659hg19UCSC Ensembl
Innerchr17:41569489..42020975hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38451948
hg19451948
hg18451487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056629
Supporting Variants
Samples
Known GenesARL17A, ARL17B, KANSL1, KANSL1-AS1, LOC644172, LRRC37A, LRRC37A2, NSFP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3723889
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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