A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373726



Internal ID21031279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108484884..108555376hg38UCSC Ensembl
chr3:108203731..108274223hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3870493
hg1970493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093312
Samples
Known GenesKIAA1524, MYH15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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