A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633893



Internal ID18932174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:80488875..80533012hg38UCSC Ensembl
Innerchr4:81410029..81454166hg19UCSC Ensembl
Innerchr4:81629053..81673190hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3844138
hg1944138
hg1844138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013945
Supporting Variants
Samples
Known GenesC4orf22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3633893
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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