A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356041



Internal ID21013594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158570217..158604746hg38UCSC Ensembl
chr3:158288006..158322535hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3834530
hg1934530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094630
Samples
Known GenesLOC100996447, MLF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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