A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899976



Internal ID22675113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155839463..155845824hg38UCSC Ensembl
chr4:156760615..156766976hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg386362
hg196362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425435
Samples
Known GenesASIC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899976
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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