A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv935357



Internal ID15882627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1405829..1733716hg38UCSC Ensembl
Innerchr20:1386473..1714362hg19UCSC Ensembl
Innerchr20:1334473..1662362hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38327888
hg19327890
hg18327890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585206
Supporting Variants
Samples
Known GenesNSFL1C, SIRPB1, SIRPB2, SIRPD, SIRPG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv935357
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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