A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633829



Internal ID18932110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:76855052..76866051hg38UCSC Ensembl
Innerchr4:77776205..77787204hg19UCSC Ensembl
Innerchr4:77995229..78006228hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3811000
hg1911000
hg1811000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014089
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3633829
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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