A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv837



Internal ID15544776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:126976982..127011903hg38UCSC Ensembl
Outerchr9:129739261..129774182hg19UCSC Ensembl
Outerchr9:128779082..128814003hg18UCSC Ensembl
Outerchr9:126818815..126853736hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386073
hg196073
hg186073
hg176073
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6721
Supporting Variants
SamplesNA19240
Known GenesRALGPS1
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)nssv837
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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