A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007481



Internal ID21916824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8526570..8553866hg38UCSC Ensembl
chr6:8526803..8554099hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3827297
hg1927297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564837
Samples
Known GenesLOC100506207
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007481
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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