A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444594



Internal ID21102147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30621541..30866516hg38UCSC Ensembl
chr10:30910470..31155445hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38244976
hg19244976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184896
Samples
Known GenesLYZL2, SVILP1, ZNF438
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444594
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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