A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4344



Internal ID15539071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:12564484..12605383hg38UCSC Ensembl
Outerchr19:12675298..12716197hg19UCSC Ensembl
Outerchr19:12536298..12577197hg18UCSC Ensembl
Outerchr19:12536298..12577197hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3840900
hg1940900
hg1840900
hg1740900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2419
Supporting Variants
SamplesNA12878
Known GenesZNF490
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)nssv4344
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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