A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386026



Internal ID21043579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89933463..90031783hg38UCSC Ensembl
chr4:90854614..90952934hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3898321
hg1998321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5356n223
Supporting Variantsnssv18122530
Samples
Known GenesMMRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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