A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5722



Internal ID15543696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:8712895..8779816hg38UCSC Ensembl
Outerchr19:8823242..8890492hg19UCSC Ensembl
Outerchr19:8684242..8751492hg18UCSC Ensembl
Outerchr19:8684242..8751492hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3866922
hg1967251
hg1867251
hg1767251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2402
Supporting Variants
SamplesNA19129
Known GenesOR2Z1
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)nssv5722
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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