A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967



Internal ID15550829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:138303494..138331099hg38UCSC Ensembl
Outerchr7:137988239..138015844hg19UCSC Ensembl
Outerchr7:137638779..137666384hg18UCSC Ensembl
Outerchr7:137445494..137473099hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3827606
hg1927606
hg1827606
hg1727606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1687
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)nsv5967
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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