A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8189



Internal ID15188989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:168297982..168339071hg38UCSC Ensembl
Outerchr5:167724987..167766076hg19UCSC Ensembl
Outerchr5:167657565..167698654hg18UCSC Ensembl
Outerchr5:167657565..167698654hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3841090
hg1941090
hg1841090
hg1741090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5119
Supporting Variants
SamplesNA12156
Known GenesWWC1
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)nssv8189
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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