A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7805



Internal ID15536059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:49632340..49643154hg38UCSC Ensembl
Outerchr3:49669773..49680587hg19UCSC Ensembl
Outerchr3:49644777..49655591hg18UCSC Ensembl
Outerchr3:49644777..49655591hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3810815
hg1910815
hg1810815
hg1710815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3812
Supporting Variants
SamplesNA12156
Known GenesBSN
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)nssv7805
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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