A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005776



Internal ID20572816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9260801..9262500hg38UCSC Ensembl
chr12:9413397..9415096hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474401
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005776
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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