A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3878n100



Internal ID22789965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76782382..76901525hg38UCSC Ensembl
chr2:77009508..77128651hg19UCSC Ensembl
chr2:76863016..76982159hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38119144
hg19119144
hg18119144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005091, nsv1006086, nsv1007648
Samples
Known GenesLRRTM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3878n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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