A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471



Internal ID15551384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:7616358..7648836hg38UCSC Ensembl
Outerchr9:7616358..7648836hg19UCSC Ensembl
Outerchr9:7606358..7638836hg18UCSC Ensembl
Outerchr9:7606358..7638836hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg387008
hg197008
hg187008
hg177008
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10653
SamplesNA18956
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)nsv6471
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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