A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964666



Internal ID22739601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32979046..32979046hg38UCSC Ensembl
chr6:32946823..32946823hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440628
Samples
Known GenesBRD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964666
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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