A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8056



Internal ID15535808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:3744591..3789711hg38UCSC Ensembl
Outerchr5:3744705..3789825hg19UCSC Ensembl
Outerchr5:3797705..3842825hg18UCSC Ensembl
Outerchr5:3797705..3842825hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3845121
hg1945121
hg1845121
hg1745121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4685
Supporting Variants
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)nssv8056
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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