A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5733



Internal ID15543683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19715752..19736929hg38UCSC Ensembl
Outerchr19:19826561..19847738hg19UCSC Ensembl
Outerchr19:19687561..19708738hg18UCSC Ensembl
Outerchr19:19687561..19708738hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3821178
hg1921178
hg1821178
hg1721178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2436
Supporting Variants
SamplesNA19129
Known GenesZNF14
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)nssv5733
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer