A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584746



Internal ID18536341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:35217473..35319358hg38UCSC Ensembl
Innerchr20:33805276..33907161hg19UCSC Ensembl
Innerchr20:33268937..33370575hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38101886
hg19101886
hg18101639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059168
Supporting Variants
Samples
Known GenesEIF6, FAM83C, MMP24, MMP24-AS1, UQCC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584746
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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