A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5721



Internal ID15197012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:8275976..8300172hg38UCSC Ensembl
Outerchr19:8340860..8365056hg19UCSC Ensembl
Outerchr19:8246860..8271056hg18UCSC Ensembl
Outerchr19:8246860..8271056hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3824197
hg1924197
hg1824197
hg1724197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2401
Supporting Variants
SamplesNA19129
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)nssv5721
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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