A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567518



Internal ID21759561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28742324..28742421hg38UCSC Ensembl
chr7:28781941..28782038hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007272
Supporting Variants
Samples
Known GenesCREB5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567518
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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