A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3544175



Internal ID18842456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41266750..41295777hg38UCSC Ensembl
Innerchr17:39423002..39452029hg19UCSC Ensembl
Innerchr17:36676528..36705555hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3829028
hg1929028
hg1829028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059164
Supporting Variants
Samples
Known GenesKRTAP9-7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3544175
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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