A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901997



Internal ID22677150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:178005724..178006240hg38UCSC Ensembl
chr4:178926878..178927394hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901997
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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