A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561587



Internal ID21885942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12017664..12023967hg38UCSC Ensembl
chr6:12017897..12024200hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg386304
hg196304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005477
Supporting Variants
Samples
Known GenesHIVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561587
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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