A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584650



Internal ID18536245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:21568712..22314413hg38UCSC Ensembl
Innerchr20:21549350..22295051hg19UCSC Ensembl
Innerchr20:21497350..22243051hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38745702
hg19745702
hg18745702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058137
Supporting Variants
Samples
Known GenesLOC100270679, PAX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584650
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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