A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6897n54



Internal ID22774792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:56475360..56675574hg38UCSC Ensembl
chr2:56702495..56902709hg19UCSC Ensembl
chr2:56555999..56756213hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38200215
hg19200215
hg18200215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582051, nsv582050
Samples
Known GenesRNU6-35P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6897n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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