A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507660



Internal ID22565609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144872905..144878089hg38UCSC Ensembl
chr8:146098290..146103474hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg385185
hg195185
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860561
Supporting Variants
Samples
Known GenesZNF250
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507660
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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