A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9683



Internal ID15540120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:17423282..17479543hg38UCSC Ensembl
Outerchr6:17423513..17479774hg19UCSC Ensembl
Outerchr6:17531492..17587753hg18UCSC Ensembl
Outerchr6:17531492..17587753hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3856262
hg1956262
hg1856262
hg1756262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5214
Supporting Variants
SamplesNA18507
Known GenesCAP2
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)nssv9683
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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