A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978663



Internal ID20545703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126084356..126091076hg38UCSC Ensembl
chr10:127772925..127779645hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg386721
hg196721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444921
Supporting Variants
Samples
Known GenesADAM12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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