A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6708



Internal ID15551644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:123834565..123859793hg38UCSC Ensembl
Outerchr9:126596844..126622072hg19UCSC Ensembl
Outerchr9:125636665..125661893hg18UCSC Ensembl
Outerchr9:123676398..123701626hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3812340
hg1912340
hg1812340
hg1712340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9473
SamplesNA18517
Known GenesDENND1A
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)nsv6708
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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