A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005477



Internal ID21914820
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 StatusM
Merged Variants
Supporting Variantsnssv17561587
Samples
Known GenesHIVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005477
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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