A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6835n54



Internal ID22774730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44240163..44240905hg38UCSC Ensembl
chr2:44467302..44468044hg19UCSC Ensembl
chr2:44320806..44321548hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38743
hg19743
hg18743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv581686, nsv581684
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6835n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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