A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505014



Internal ID22562958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113934238..113938512hg38UCSC Ensembl
chr8:114946467..114950741hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg384275
hg194275
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865040
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505014
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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