A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352198



Internal ID22577867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79274031..79274087hg38UCSC Ensembl
chr10:81033788..81033844hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918227
Supporting Variants
Samples
Known GenesZMIZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352198
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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