A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7431



Internal ID15189747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:18966623..19011770hg38UCSC Ensembl
Outerchr19:19077432..19122579hg19UCSC Ensembl
Outerchr19:18938432..18983579hg18UCSC Ensembl
Outerchr19:18938432..18983579hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3845148
hg1945148
hg1845148
hg1745148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2435
Supporting Variants
SamplesNA12156
Known GenesSUGP2
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)nssv7431
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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