A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998899



Internal ID20565939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30056183..30062088hg38UCSC Ensembl
chr12:30209116..30215021hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg385906
hg195906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468875
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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