A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9853



Internal ID15193238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:8258600..8306826hg38UCSC Ensembl
Outerchr19:8323484..8371710hg19UCSC Ensembl
Outerchr19:8229484..8277710hg18UCSC Ensembl
Outerchr19:8229484..8277710hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3848227
hg1948227
hg1848227
hg1748227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2401
Supporting Variants
SamplesNA18507
Known GenesCD320, CERS4
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)nssv9853
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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