A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4350



Internal ID15539077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29897281..29918857hg38UCSC Ensembl
Outerchr19:30388188..30409764hg19UCSC Ensembl
Outerchr19:35080028..35101604hg18UCSC Ensembl
Outerchr19:35080028..35101604hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3821577
hg1921577
hg1821577
hg1721577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2457
Supporting Variants
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)nssv4350
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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