A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889891



Internal ID22664913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142408351..142409290hg38UCSC Ensembl
chr4:143329504..143330443hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423087
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889891
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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