A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960602



Internal ID18595850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41374325..41383879hg38UCSC Ensembl
Innerchr17:39530577..39540131hg19UCSC Ensembl
Innerchr17:36784103..36793657hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg389555
hg199555
hg189555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758486
SamplesHGDP00927
Known GenesKRT34
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960602
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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