A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926295



Internal ID22701522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74698110..74701813hg38UCSC Ensembl
chr11:74409155..74412858hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383704
hg193704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367174
Samples
Known GenesCHRDL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926295
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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