A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150645



Internal ID15506691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:30452770..30482476hg38UCSC Ensembl
Innerchr19:30943677..30973383hg19UCSC Ensembl
Innerchr19:35635517..35665223hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3829707
hg1929707
hg1829707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579284
Supporting Variants
Samples1780854128_A
Known GenesZNF536
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150645
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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