A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001834



Internal ID21911177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100358060..100363198hg38UCSC Ensembl
chr7:99955683..99960821hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385139
hg195139
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568170
Samples
Known GenesPILRB, STAG3L5P-PVRIG2P-PILRB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001834
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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