A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012089



Internal ID21921432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151141676..151141729hg38UCSC Ensembl
chr5:150521237..150521290hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562843
Samples
Known GenesANXA6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012089
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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