A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899634



Internal ID22674765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156655793..156687464hg38UCSC Ensembl
chr4:157576945..157608616hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3831672
hg1931672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899634
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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