A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014905



Internal ID21924248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131863282..131863386hg38UCSC Ensembl
chr7:131548041..131548145hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014905
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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