A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2427



Internal ID15540705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:162788329..162921273hg38UCSC Ensembl
Outerchr3:162506117..162639061hg19UCSC Ensembl
Outerchr3:163988811..164121755hg18UCSC Ensembl
Outerchr3:163988819..164121763hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38132945
hg19132945
hg18132945
hg17132945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4093
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)nssv2427
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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