A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4262



Internal ID15548954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:19238813..19283039hg38UCSC Ensembl
Outerchr4:19240436..19284662hg19UCSC Ensembl
Outerchr4:18849534..18893760hg18UCSC Ensembl
Outerchr4:18916705..18960931hg17UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3844227
hg1944227
hg1844227
hg1744227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2457
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)nsv4262
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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