A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067562



Internal ID21456410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117126450..117126533hg38UCSC Ensembl
chr10:118885961..118886044hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590581
Supporting Variants
SamplesHG02492
Known GenesKIAA1598
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067562
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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