A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5146n100



Internal ID22791233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16333756..16362286hg38UCSC Ensembl
chr4:16335379..16363909hg19UCSC Ensembl
chr4:15944477..15973007hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3828531
hg1928531
hg1828531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000404, nsv1014580, nsv1002051
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)dgv5146n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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