A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6646



Internal ID15551576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:102737046..102768434hg38UCSC Ensembl
Outerchr9:105499328..105530716hg19UCSC Ensembl
Outerchr9:104539149..104570537hg18UCSC Ensembl
Outerchr9:102578883..102610271hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg387871
hg197871
hg187871
hg177871
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5173
SamplesNA19129
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)nsv6646
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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