A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6700



Internal ID15551636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:120896969..120930014hg38UCSC Ensembl
Outerchr9:123659247..123692292hg19UCSC Ensembl
Outerchr9:122699068..122732113hg18UCSC Ensembl
Outerchr9:120738801..120771846hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg386392
hg196392
hg186392
hg176392
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8660
SamplesNA12156
Known GenesTRAF1
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)nsv6700
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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