A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837713



Internal ID22612648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142509481..142518910hg38UCSC Ensembl
chr4:143430634..143440063hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg389430
hg199430
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499597
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837713
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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