A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440713



Internal ID21098266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86472863..86580805hg38UCSC Ensembl
chr10:88232620..88340562hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38107943
hg19107943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182890
Samples
Known GenesWAPAL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440713
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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