A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633902



Internal ID18932183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:84271901..84334256hg38UCSC Ensembl
Innerchr4:85193054..85255409hg19UCSC Ensembl
Innerchr4:85412078..85474433hg18UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3862356
hg1962356
hg1862356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998617
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)nssv3633902
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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