A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9472



Internal ID15540186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:88193967..88213874hg38UCSC Ensembl
Outerchr9:90808882..90828789hg19UCSC Ensembl
Outerchr9:89998702..90018609hg18UCSC Ensembl
Outerchr9:88038436..88058343hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3814073
hg1914073
hg1814073
hg1714073
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6603
Supporting Variants
SamplesNA18517
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)nssv9472
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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