A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2220



Internal ID15194817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:36345372..36359341hg38UCSC Ensembl
Outerchr19:36836274..36850243hg19UCSC Ensembl
Outerchr19:41528114..41542083hg18UCSC Ensembl
Outerchr19:41528114..41542083hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3813970
hg1913970
hg1813970
hg1713970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2474
Supporting Variants
SamplesNA18555
Known GenesZFP14
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)nssv2220
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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