A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007561



Internal ID21916904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5550317..5550423hg38UCSC Ensembl
chr7:5589948..5590054hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563537
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007561
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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