A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3715



Internal ID15538443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:38239733..38274821hg38UCSC Ensembl
Outerchr9:38239730..38274818hg19UCSC Ensembl
Outerchr9:38229730..38264818hg18UCSC Ensembl
Outerchr9:38229730..38264818hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg384660
hg194660
hg184660
hg174660
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536
Supporting Variants
SamplesNA12878
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)nssv3715
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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