A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011598



Internal ID21920941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87751384..87751580hg38UCSC Ensembl
chr6:88461102..88461298hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011598
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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