A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122073



Internal ID21474344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174787472..174787569hg38UCSC Ensembl
chr4:175708623..175708720hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582519
Supporting Variants
SamplesHG03371
Known GenesGLRA3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122073
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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