A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501



Internal ID15551417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:22454235..22487341hg38UCSC Ensembl
Outerchr9:22454234..22487340hg19UCSC Ensembl
Outerchr9:22444234..22477340hg18UCSC Ensembl
Outerchr9:22444234..22477340hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg386330
hg196330
hg186330
hg176330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8594
SamplesNA12156
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)nsv6501
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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