A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925767



Internal ID22700994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46757695..46757994hg38UCSC Ensembl
chr11:46779245..46779544hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364700
Samples
Known GenesCKAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925767
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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