A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079624



Internal ID21988857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74204025..74204025hg38UCSC Ensembl
chr7:73618355..73618355hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079624
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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