A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412356



Internal ID21069909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146759361..146760039hg38UCSC Ensembl
chr5:146138924..146139602hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126067
Samples
Known GenesPPP2R2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412356
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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