A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008877



Internal ID21918220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88203750..88203802hg38UCSC Ensembl
chr5:87499567..87499619hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556470
Samples
Known GenesTMEM161B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008877
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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