A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888654



Internal ID22663662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61496556..61496854hg38UCSC Ensembl
chr4:62362274..62362572hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410171
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888654
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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