A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015767



Internal ID21925110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130591097..130591154hg38UCSC Ensembl
chr7:130275366..130275423hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570787
Samples
Known GenesCOPG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015767
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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