A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv736826



Internal ID15684096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:211577866..211579293hg38UCSC Ensembl
Innerchr1:211751208..211752635hg19UCSC Ensembl
Innerchr1:209817831..209819258hg18UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg381428
hg191428
hg181428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549126
Supporting Variants
Samples
Known GenesSLC30A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv736826
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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