A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365780



Internal ID22591449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71861641..71861959hg38UCSC Ensembl
chr10:73621398..73621716hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920595
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365780
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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