A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016292



Internal ID21925635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77261610..77307977hg38UCSC Ensembl
chr7:76890927..76937294hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3846368
hg1946368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569352
Samples
Known GenesCCDC146
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016292
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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