A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9621n54



Internal ID22777516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16179136..16179950hg38UCSC Ensembl
chr5:16179245..16180059hg19UCSC Ensembl
chr5:16232245..16233059hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38815
hg19815
hg18815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597302, nsv597304
Samples
Known GenesMARCH11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9621n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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