A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6739



Internal ID15204992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:132135179..132166954hg38UCSC Ensembl
Outerchr9:135010566..135042341hg19UCSC Ensembl
Outerchr9:134000387..134032162hg18UCSC Ensembl
Outerchr9:132040120..132071895hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg387508
hg197508
hg187508
hg177508
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5185
SamplesNA19129
Known GenesNTNG2
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)nsv6739
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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