A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997482



Internal ID20564522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:127434610..127589770hg38UCSC Ensembl
chr12:127919155..128074315hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38155161
hg19155161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481032
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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