A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2206



Internal ID15194803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:8263488..8300867hg38UCSC Ensembl
Outerchr19:8328372..8365751hg19UCSC Ensembl
Outerchr19:8234372..8271751hg18UCSC Ensembl
Outerchr19:8234372..8271751hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3837380
hg1937380
hg1837380
hg1737380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2401
Supporting Variants
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)nssv2206
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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