A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358794



Internal ID22584463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4422235..4423082hg38UCSC Ensembl
chr10:4464427..4465274hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912935
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358794
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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