A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391579



Internal ID21049132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142129819..142130294hg38UCSC Ensembl
chr4:143050972..143051447hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108811
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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