A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414702



Internal ID21072255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147664168..147664566hg38UCSC Ensembl
chr5:147043731..147044129hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126135
Samples
Known GenesJAKMIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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