A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000610



Internal ID21909953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30115862..30115917hg38UCSC Ensembl
chr7:30155478..30155533hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564651
Samples
Known GenesPLEKHA8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000610
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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