A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005884



Internal ID20572924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95883981..95885849hg38UCSC Ensembl
chr12:96277759..96279627hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381869
hg191869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473628
Supporting Variants
Samples
Known GenesCCDC38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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