A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075448



Internal ID21984681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32472533..32472533hg38UCSC Ensembl
chr7:32512145..32512145hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075448
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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