A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504897



Internal ID22562841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108514400..108521948hg38UCSC Ensembl
chr8:109526629..109534177hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg387549
hg197549
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848591
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504897
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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