A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3544177



Internal ID18495772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41266750..41322116hg38UCSC Ensembl
Innerchr17:39423002..39478368hg19UCSC Ensembl
Innerchr17:36676528..36731894hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3855367
hg1955367
hg1855367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055426
Supporting Variants
Samples
Known GenesKRTAP16-1, KRTAP17-1, KRTAP29-1, KRTAP9-7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3544177
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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