A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6808n54



Internal ID22774703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:41001448..41035363hg38UCSC Ensembl
chr2:41228588..41262503hg19UCSC Ensembl
chr2:41082092..41116007hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3833916
hg1933916
hg1833916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv581544, nsv581548, nsv581549, nsv581547
SamplesNINDS_166, HGDP00625
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6808n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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