A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2615



Internal ID15540498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:133019028..133033610hg38UCSC Ensembl
Outerchr6:133340167..133354749hg19UCSC Ensembl
Outerchr6:133381860..133396442hg18UCSC Ensembl
Outerchr6:133381860..133396442hg17UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3814583
hg1914583
hg1814583
hg1714583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481
Supporting Variants
SamplesNA18555
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)nssv2615
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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