A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6755n54



Internal ID20140179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33540105..33541741hg38UCSC Ensembl
chr2:33765172..33766808hg19UCSC Ensembl
chr2:33618676..33620312hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg381637
hg191637
hg181637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv581316, nsv581329, nsv581311, nsv581323, nsv581312, nsv581318, nsv581319, nsv581322, nsv581320, nsv581326, nsv581315, nsv581324, nsv581327, nsv581314
Samples
Known GenesRASGRP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6755n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss126
Observed Complex0
Frequencyn/a


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