A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2459



Internal ID15547022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:30664333..30696992hg38UCSC Ensembl
Outerchr19:31155240..31187899hg19UCSC Ensembl
Outerchr19:35847080..35879739hg18UCSC Ensembl
Outerchr19:35847080..35879739hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg387081
hg197081
hg187081
hg177081
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4352
SamplesNA12878
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)nsv2459
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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