A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960597



Internal ID18249159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37036433..37040669hg38UCSC Ensembl
Innerchr17:35393730..35397967hg19UCSC Ensembl
Innerchr17:32467843..32472080hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384237
hg194238
hg184238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759610
SamplesHGDP00456
Known GenesAATF
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960597
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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