A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985348



Internal ID20552388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91375357..91375970hg38UCSC Ensembl
chr10:93135114..93135727hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454217
Supporting Variants
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985348
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00058


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