A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567457



Internal ID21759500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105559137..105559280hg38UCSC Ensembl
chr7:105199584..105199727hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006024
Supporting Variants
Samples
Known GenesRINT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567457
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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