A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3873n100



Internal ID22789960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76315863..76359573hg38UCSC Ensembl
chr2:76542989..76586699hg19UCSC Ensembl
chr2:76396497..76440207hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3843711
hg1943711
hg1843711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007312, nsv1008178, nsv1003728, nsv1008019, nsv1014043, nsv1011137
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)dgv3873n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer