A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv219n21



Internal ID22766411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:53248200..53324462hg38UCSC Ensembl
chr2:53475338..53551600hg19UCSC Ensembl
chr2:53328842..53405104hg18UCSC Ensembl
chr2:53386989..53463251hg17UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3876263
hg1976263
hg1876263
hg1776263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522463, nsv522095
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv219n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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