A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998951



Internal ID20565991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30732101..30733100hg38UCSC Ensembl
chr12:30885035..30886034hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461078
Supporting Variants
Samples
Known GenesCAPRIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998951
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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