A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536



Internal ID15551455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:38234691..38274821hg38UCSC Ensembl
Outerchr9:38234688..38274818hg19UCSC Ensembl
Outerchr9:38224688..38264818hg18UCSC Ensembl
Outerchr9:38224688..38264818hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg385440
hg195440
hg185440
hg175440
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3715, nssv8607
SamplesNA12156, NA12878
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)nsv6536
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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