A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv736839



Internal ID15684109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:211578592..211579752hg38UCSC Ensembl
Innerchr1:211751934..211753094hg19UCSC Ensembl
Innerchr1:209818557..209819717hg18UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg381161
hg191161
hg181161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549136
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)nssv736839
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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