A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004491



Internal ID21913834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154744622..154744938hg38UCSC Ensembl
chr5:154124182..154124498hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572407
Samples
Known GenesLARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004491
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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