A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2211



Internal ID15194808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:9385325..9429591hg38UCSC Ensembl
Outerchr19:9496001..9540267hg19UCSC Ensembl
Outerchr19:9357001..9401267hg18UCSC Ensembl
Outerchr19:9357001..9401267hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3844267
hg1944267
hg1844267
hg1744267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2412
Supporting Variants
SamplesNA18555
Known GenesZNF266
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)nssv2211
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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