A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016332



Internal ID21925675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30584616..30584692hg38UCSC Ensembl
chr7:30624232..30624308hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016332
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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