A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6265



Internal ID15537598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:20827624..20859653hg38UCSC Ensembl
Outerchr9:20827623..20859652hg19UCSC Ensembl
Outerchr9:20817623..20849652hg18UCSC Ensembl
Outerchr9:20817623..20849652hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg387412
hg197412
hg187412
hg177412
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499
Supporting Variants
SamplesNA12156
Known GenesFOCAD
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)nssv6265
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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