A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982440



Internal ID20549480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6612797..6614184hg38UCSC Ensembl
chr10:6654759..6656146hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381388
hg191388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436406
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0009


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