A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571



Internal ID15551494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:76863592..76895659hg38UCSC Ensembl
Outerchr9:79478508..79510575hg19UCSC Ensembl
Outerchr9:78668328..78700395hg18UCSC Ensembl
Outerchr9:76708062..76740129hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg387372
hg197372
hg187372
hg177372
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6284
SamplesNA12156
Known GenesPRUNE2
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)nsv6571
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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