A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572535



Internal ID21764578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37288653..37288653hg38UCSC Ensembl
chr8:37146171..37146171hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg385912
hg195912
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6062094
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572535
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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