A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997053



Internal ID21906396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37849472..37849538hg38UCSC Ensembl
chr4:37851093..37851159hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552004
Samples
Known GenesPGM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997053
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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