A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633883



Internal ID18585478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:78811314..78867614hg38UCSC Ensembl
Innerchr4:79732468..79788768hg19UCSC Ensembl
Innerchr4:79951492..80007792hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3856301
hg1956301
hg1856301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007685
Supporting Variants
Samples
Known GenesBMP2K
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3633883
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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