A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3757n100



Internal ID22789844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:34419042..34502788hg38UCSC Ensembl
chr2:34644109..34727855hg19UCSC Ensembl
chr2:34497613..34581359hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3883747
hg1983747
hg1883747
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002336, nsv1014312, nsv1009253, nsv1009517, nsv998396, nsv1010263, nsv1011728, nsv999506, nsv1005622
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)dgv3757n100
Frequency
Sample Size11257
Observed Gain66
Observed Loss0
Observed Complex0
Frequencyn/a


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