A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204863



Internal ID21343675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38074136..38074136hg38UCSC Ensembl
chr8:37931654..37931654hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939413
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204863
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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