A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9854



Internal ID15193239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:34241734..34261327hg38UCSC Ensembl
Outerchr19:34732639..34752232hg19UCSC Ensembl
Outerchr19:39424479..39444072hg18UCSC Ensembl
Outerchr19:39424479..39444072hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg388244
hg198244
hg188244
hg178244
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2468
Supporting Variants
SamplesNA18507
Known GenesKIAA0355
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)nssv9854
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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