A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9574n54



Internal ID22777469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9896051..9933108hg38UCSC Ensembl
chr5:9896163..9933220hg19UCSC Ensembl
chr5:9949163..9986220hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3837058
hg1937058
hg1837058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597084, nsv597097, nsv597095, nsv597096
Samples1780862516_A, 1780862015_A, HGDP00620, NINDS_203, HGDP00667
Known GenesLOC285692
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9574n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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