A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006792



Internal ID21916135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116277111..116277629hg38UCSC Ensembl
chr7:115917165..115917683hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006792
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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