A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002351



Internal ID21911694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159962838..159962935hg38UCSC Ensembl
chr5:159389845..159389942hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571910
Samples
Known GenesADRA1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002351
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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