A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440006



Internal ID21097559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50869201..50872000hg38UCSC Ensembl
chr10:52628961..52631760hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981513
Samples
Known GenesA1CF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440006
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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