A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367880



Internal ID21025433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64724561..64732327hg38UCSC Ensembl
chr3:64710237..64718003hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg387767
hg197767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101516
Samples
Known GenesADAMTS9-AS2, MIR548A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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