A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015576



Internal ID21924919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23543064..23543137hg38UCSC Ensembl
chr7:23582683..23582756hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576354
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015576
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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