A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904797



Internal ID22679975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64842337..64842632hg38UCSC Ensembl
chr5:64138164..64138459hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426522
Samples
Known GenesCWC27
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904797
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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