A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356983



Internal ID22582652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30930784..30930857hg38UCSC Ensembl
chr10:31219713..31219786hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923379
Supporting Variants
Samples
Known GenesZNF438
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356983
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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