A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6637



Internal ID15551566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:99490816..99517980hg38UCSC Ensembl
Outerchr9:102253098..102280262hg19UCSC Ensembl
Outerchr9:101292919..101320083hg18UCSC Ensembl
Outerchr9:99332653..99359817hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg389938
hg199938
hg189938
hg179938
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1793
SamplesNA18555
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)nsv6637
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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