A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6775



Internal ID15551718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137842688..137869167hg38UCSC Ensembl
Outerchr9:140737140..140763619hg19UCSC Ensembl
Outerchr9:139856961..139883440hg18UCSC Ensembl
Outerchr9:138012977..138039456hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg388350
hg198350
hg188350
hg178350
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv847
SamplesNA19240
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)nsv6775
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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