A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374252



Internal ID21031805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64656757..64661997hg38UCSC Ensembl
chr3:64642433..64647673hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg385241
hg195241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101510
Samples
Known GenesADAMTS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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