A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003178



Internal ID21912521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173129539..173129667hg38UCSC Ensembl
chr5:172556542..172556670hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559251
Samples
Known GenesCREBRF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003178
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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