A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980584



Internal ID20547624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129782637..129783648hg38UCSC Ensembl
chr10:131580901..131581912hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381012
hg191012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440009
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980584
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00117


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