A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897034



Internal ID22672131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56950448..56950532hg38UCSC Ensembl
chr4:57816614..57816698hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422400
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897034
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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