A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038996



Internal ID21948339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54887008..54887085hg38UCSC Ensembl
chr18:52554239..52554316hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623309
Samples
Known GenesRAB27B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038996
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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