A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9820n54



Internal ID22777715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64399566..64406514hg38UCSC Ensembl
chr5:63695393..63702341hg19UCSC Ensembl
chr5:63731149..63738097hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg386949
hg196949
hg186949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598353, nsv598354, nsv598357, nsv598358, nsv598356, nsv598355
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9820n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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