A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903667



Internal ID22678836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175750464..175758814hg38UCSC Ensembl
chr4:176671615..176679965hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg388351
hg198351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425399
Samples
Known GenesGPM6A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903667
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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