A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361840



Internal ID22587509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5471575..5476312hg38UCSC Ensembl
chr10:5513538..5518275hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg384738
hg194738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361840
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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