A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4028n100



Internal ID22790115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98238544..98264877hg38UCSC Ensembl
chr2:98855007..98881340hg19UCSC Ensembl
chr2:98221439..98247772hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3826334
hg1926334
hg1826334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003683, nsv1014147, nsv999884, nsv1008771, nsv1010376, nsv1005509
Samples
Known GenesVWA3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4028n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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