A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901975



Internal ID22677128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:132005314..132032414hg38UCSC Ensembl
chr4:132926469..132953569hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3827101
hg1927101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901975
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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