A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633900



Internal ID18932181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:83230703..83240797hg38UCSC Ensembl
Innerchr4:84151856..84161950hg19UCSC Ensembl
Innerchr4:84370880..84380974hg18UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3810095
hg1910095
hg1810095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009230
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)nssv3633900
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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