A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6683n54



Internal ID22774578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9304549..9306151hg38UCSC Ensembl
chr2:9444678..9446280hg19UCSC Ensembl
chr2:9362129..9363731hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381603
hg191603
hg181603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580923, nsv580918, nsv580917
Samples
Known GenesASAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6683n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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