A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8673



Internal ID15535191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133859019..133862304hg38UCSC Ensembl
Outerchr9:136724141..136727426hg19UCSC Ensembl
Outerchr9:135713962..135717247hg18UCSC Ensembl
Outerchr9:133753695..133756980hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg387218
hg197218
hg187218
hg177218
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6750
Supporting Variants
SamplesNA12156
Known GenesVAV2
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)nssv8673
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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