A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907502



Internal ID22682711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53253255..53253308hg38UCSC Ensembl
chr6:53118053..53118106hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907502
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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