A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985385



Internal ID20552425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91980437..91981108hg38UCSC Ensembl
chr10:93740194..93740865hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442069
Supporting Variants
Samples
Known GenesBTAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985385
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00047


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