A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10988n54



Internal ID22778883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160610992..160647288hg38UCSC Ensembl
chr6:161032024..161068320hg19UCSC Ensembl
chr6:160952014..160988310hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3836297
hg1936297
hg1836297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604999, nsv605002, nsv605004, nsv605003, nsv605000, nsv605001
Samples
Known GenesLPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10988n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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