A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1437



Internal ID15544270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:12581688..12594612hg38UCSC Ensembl
Outerchr19:12692502..12705426hg19UCSC Ensembl
Outerchr19:12553502..12566426hg18UCSC Ensembl
Outerchr19:12553502..12566426hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812925
hg1912925
hg1812925
hg1712925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2419
Supporting Variants
SamplesNA19240
Known GenesZNF490
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)nssv1437
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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