A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6621



Internal ID15551549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:94213901..94220228hg38UCSC Ensembl
Outerchr9:96976183..96982510hg19UCSC Ensembl
Outerchr9:96016004..96022331hg18UCSC Ensembl
Outerchr9:94055738..94062065hg17UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg384606
hg194606
hg184606
hg174606
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731
SamplesNA12878
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)nsv6621
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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