A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018413



Internal ID21927756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116754920..116754996hg38UCSC Ensembl
chr7:116394974..116395050hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557872
Samples
Known GenesMET
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018413
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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