A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9813n54



Internal ID22777708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61331739..61334076hg38UCSC Ensembl
chr5:60627566..60629903hg19UCSC Ensembl
chr5:60663323..60665660hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg382338
hg192338
hg182338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598320, nsv598321
Samples
Known GenesZSWIM6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9813n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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