A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891064



Internal ID22666097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63367945..63369184hg38UCSC Ensembl
chr6:64077850..64079089hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448470
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891064
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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