A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4349



Internal ID15539076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29452609..29467183hg38UCSC Ensembl
Outerchr19:29943516..29958090hg19UCSC Ensembl
Outerchr19:34635356..34649930hg18UCSC Ensembl
Outerchr19:34635356..34649930hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3814575
hg1914575
hg1814575
hg1714575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2455
Supporting Variants
SamplesNA12878
Known GenesLOC284395
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)nssv4349
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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