A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5159n100



Internal ID22791246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25552260..25576647hg38UCSC Ensembl
chr4:25553882..25578269hg19UCSC Ensembl
chr4:25162980..25187367hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3824388
hg1924388
hg1824388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999832, nsv1002989, nsv998183
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)dgv5159n100
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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