A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000437



Internal ID20567478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45950601..45951500hg38UCSC Ensembl
chr12:46344384..46345283hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461408
Supporting Variants
Samples
Known GenesSCAF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00037


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