A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2212



Internal ID15541495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19705049..19737059hg38UCSC Ensembl
Outerchr19:19815858..19847868hg19UCSC Ensembl
Outerchr19:19676858..19708868hg18UCSC Ensembl
Outerchr19:19676858..19708868hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3832011
hg1932011
hg1832011
hg1732011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2436
Supporting Variants
SamplesNA18555
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)nssv2212
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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