A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581



Internal ID15551505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:81388534..81417933hg38UCSC Ensembl
Outerchr9:84003449..84032848hg19UCSC Ensembl
Outerchr9:83193269..83222668hg18UCSC Ensembl
Outerchr9:81233003..81262402hg17UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3810104
hg1910104
hg1810104
hg1710104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10673
SamplesNA18956
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv6581
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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