A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv531



Internal ID15197981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:22151685..22185285hg38UCSC Ensembl
Outerchr6:22151914..22185514hg19UCSC Ensembl
Outerchr6:22259893..22293493hg18UCSC Ensembl
Outerchr6:22259893..22293493hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3833601
hg1933601
hg1833601
hg1733601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5223
Supporting Variants
SamplesNA19240
Known GenesCASC15
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)nssv531
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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