A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549131



Internal ID15989854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:211578364..211579405hg38UCSC Ensembl
Innerchr1:211751706..211752747hg19UCSC Ensembl
Innerchr1:209818329..209819370hg18UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg381042
hg191042
hg181042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv802n54
Supporting Variantsnssv736832
Samples
Known GenesSLC30A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549131
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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