A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963090



Internal ID15910360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52435769..52444412hg38UCSC Ensembl
Innerchr3:52469785..52478428hg19UCSC Ensembl
Innerchr3:52444825..52453468hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg388644
hg198644
hg188644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590303
Supporting Variants
Samples
Known GenesSEMA3G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963090
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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