A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367224



Internal ID21024777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155431146..155474962hg38UCSC Ensembl
chr3:155148935..155192751hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3843817
hg1943817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367224
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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