A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506668



Internal ID22564616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43006475..43020803hg38UCSC Ensembl
chr8:42861618..42875946hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3814329
hg1914329
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852098
Supporting Variants
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506668
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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