A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505614



Internal ID22563558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11627628..11630177hg38UCSC Ensembl
chr8:11485137..11487686hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382550
hg192550
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866564
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505614
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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