A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578368



Internal ID21770411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105536044..105536044hg38UCSC Ensembl
chr8:106548272..106548272hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074606
Supporting Variants
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578368
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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