A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6692



Internal ID15551627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:118618643..118645307hg38UCSC Ensembl
Outerchr9:121380921..121407585hg19UCSC Ensembl
Outerchr9:120420742..120447406hg18UCSC Ensembl
Outerchr9:118460475..118487139hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg384938
hg194938
hg184938
hg174938
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9771, nssv831, nssv3746
SamplesNA18507, NA12878, NA19240
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)nsv6692
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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