A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382678



Internal ID21040231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99593461..99593997hg38UCSC Ensembl
chr4:100514618..100515154hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121335
Samples
Known GenesMTTP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382678
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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