A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5611n54



Internal ID20139035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45511832..45520038hg38UCSC Ensembl
chr17:43589198..43597404hg19UCSC Ensembl
chr17:40944981..40953187hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg388207
hg198207
hg188207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575113, nsv575107, nsv575115, nsv575112, nsv575114, nsv575108
Samples
Known GenesLRRC37A4P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5611n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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