A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011199



Internal ID21920542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139452250..139481030hg38UCSC Ensembl
chr7:139136996..139165776hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3828781
hg1928781
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577027
Samples
Known GenesKLRG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011199
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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