A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430707



Internal ID22488577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67403827..67403827hg38UCSC Ensembl
chr8:68316062..68316062hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5949237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430707
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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