A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006930



Internal ID21916273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24545837..24546251hg38UCSC Ensembl
chr7:24585456..24585870hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006930
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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