A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4682



Internal ID15549416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:3542477..3587440hg38UCSC Ensembl
Outerchr5:3542591..3587554hg19UCSC Ensembl
Outerchr5:3595591..3640554hg18UCSC Ensembl
Outerchr5:3595591..3640554hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3844964
hg1944964
hg1844964
hg1744964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8055
SamplesNA12156
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)nsv4682
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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