A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6579



Internal ID15537284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:112293744..112344693hg38UCSC Ensembl
Outerchr13:112948058..112999007hg19UCSC Ensembl
Outerchr13:111996059..112047008hg18UCSC Ensembl
Outerchr13:111996059..112047008hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3850950
hg1950950
hg1850950
hg1750950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1189
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)nssv6579
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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