A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569546



Internal ID21761589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77241016..77241074hg38UCSC Ensembl
chr7:76870333..76870391hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001226
Supporting Variants
Samples
Known GenesCCDC146
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569546
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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