A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361520



Internal ID21019073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64858159..64858806hg38UCSC Ensembl
chr3:64843834..64844481hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101532
Samples
Known GenesADAMTS9-AS2, MIR548A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361520
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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