A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429378



Internal ID21086931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139446604..139469707hg38UCSC Ensembl
chr7:139131350..139154453hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3823104
hg1923104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229093
Samples
Known GenesKLRG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429378
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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