A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18003216



Internal ID20570256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:70933860..70934412hg38UCSC Ensembl
chr12:71327640..71328192hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468674
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18003216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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