A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2215



Internal ID15541498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29894777..29902843hg38UCSC Ensembl
Outerchr19:30385684..30393750hg19UCSC Ensembl
Outerchr19:35077524..35085590hg18UCSC Ensembl
Outerchr19:35077524..35085590hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg388067
hg198067
hg188067
hg178067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2457
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)nssv2215
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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