A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985809



Internal ID20552849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:986806..1028381hg38UCSC Ensembl
chr10:1032746..1074321hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3841576
hg1941576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450672
Supporting Variants
Samples
Known GenesGTPBP4, IDI2, IDI2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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