A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505952



Internal ID22563897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32158246..32191408hg38UCSC Ensembl
chr8:32015762..32048924hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3833163
hg1933163
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855038
Supporting Variants
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505952
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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