A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4061n100



Internal ID22790148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:122916985..123005638hg38UCSC Ensembl
chr2:123674561..123763214hg19UCSC Ensembl
chr2:123391031..123479684hg18UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3888654
hg1988654
hg1888654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007695, nsv1010654
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)dgv4061n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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