A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015560



Internal ID21924903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101098126..101099280hg38UCSC Ensembl
chr6:101546002..101547156hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015560
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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