A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566958



Internal ID21759001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74369854..74370155hg38UCSC Ensembl
chr7:73784184..73784485hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008036
Supporting Variants
Samples
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566958
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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