A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995663



Internal ID20562703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103786400..103790655hg38UCSC Ensembl
chr12:104180178..104184433hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg384256
hg194256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457628
Supporting Variants
Samples
Known GenesNT5DC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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