A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893511



Internal ID22668572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71402568..71402698hg38UCSC Ensembl
chr6:72112271..72112401hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893511
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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