A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397769



Internal ID21055322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94090014..94099508hg38UCSC Ensembl
chr5:93425719..93435213hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg389495
hg199495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136423
Samples
Known GenesFAM172A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397769
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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