A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997285



Internal ID20564325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124772186..124774304hg38UCSC Ensembl
chr12:125256732..125258850hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg382119
hg192119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483814
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997285
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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