A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573522



Internal ID21765565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77705421..77705569hg38UCSC Ensembl
chr7:77334738..77334886hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018692
Supporting Variants
Samples
Known GenesRSBN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573522
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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