A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008049



Internal ID21917392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74000388..74009389hg38UCSC Ensembl
chr7:73414718..73423719hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg389002
hg199002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008049
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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