A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837935



Internal ID22612870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:129140910..129144943hg38UCSC Ensembl
chr4:130062065..130066098hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg384034
hg194034
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837935
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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