A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998887



Internal ID20565927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29941831..29984481hg38UCSC Ensembl
chr12:30094764..30137414hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3842651
hg1942651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471063
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998887
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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