A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5728



Internal ID15197005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:11927167..11936322hg38UCSC Ensembl
Outerchr19:12037982..12047137hg19UCSC Ensembl
Outerchr19:11898982..11908137hg18UCSC Ensembl
Outerchr19:11898982..11908137hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg389156
hg199156
hg189156
hg179156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2417
Supporting Variants
SamplesNA19129
Known GenesZNF700
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)nssv5728
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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