A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567997



Internal ID21760040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54759207..54759452hg38UCSC Ensembl
chr7:54826900..54827145hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017873
Supporting Variants
Samples
Known GenesSEC61G
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567997
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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