A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435775



Internal ID22493645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61794266..61794266hg38UCSC Ensembl
chr8:62706825..62706825hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959057
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435775
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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