A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510



Internal ID15551427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:26607671..26641968hg38UCSC Ensembl
Outerchr9:26607669..26641966hg19UCSC Ensembl
Outerchr9:26597669..26631966hg18UCSC Ensembl
Outerchr9:26597669..26631966hg17UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg386694
hg196694
hg186694
hg176694
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv795
SamplesNA19240
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)nsv6510
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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