A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001505



Internal ID21910848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164945530..164957381hg38UCSC Ensembl
chr6:165359019..165370870hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3811852
hg1911852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001505
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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