A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003618



Internal ID21912961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46996243..46998191hg38UCSC Ensembl
chr6:46963980..46965928hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg381949
hg191949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560920
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003618
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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