A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979145



Internal ID20546185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21177094..21178193hg38UCSC Ensembl
chr10:21466023..21467122hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450071
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979145
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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