A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078198



Internal ID21987431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117097908..117097908hg38UCSC Ensembl
chr7:116737962..116737962hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558133
Samples
Known GenesST7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078198
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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