A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059164



Internal ID19148383
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 StatusM
Merged Variantsdgv3170n100
Supporting Variantsnssv3544175, nssv3544176
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)nsv1059164
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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