A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1790



Internal ID15541073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:87895147..87926417hg38UCSC Ensembl
Outerchr9:90510062..90541332hg19UCSC Ensembl
Outerchr9:89699882..89731152hg18UCSC Ensembl
Outerchr9:87739616..87770886hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg388736
hg198736
hg188736
hg178736
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6599
Supporting Variants
SamplesNA18555
Known GenesSPATA31C1
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)nssv1790
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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