A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6773



Internal ID15537090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:12549691..12589924hg38UCSC Ensembl
Outerchr19:12660505..12700738hg19UCSC Ensembl
Outerchr19:12521505..12561738hg18UCSC Ensembl
Outerchr19:12521505..12561738hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3840234
hg1940234
hg1840234
hg1740234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2419
Supporting Variants
SamplesNA12156
Known GenesZNF490, ZNF564
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)nssv6773
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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