A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005062



Internal ID21914405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54978958..54980110hg38UCSC Ensembl
chr7:55046651..55047803hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg381153
hg191153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572464
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005062
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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