A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351784



Internal ID22577453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28844313..28844376hg38UCSC Ensembl
chr10:29133242..29133305hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916955
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351784
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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