A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999174



Internal ID20566214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:126060466..126420326hg38UCSC Ensembl
chr12:126545012..126904872hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38359861
hg19359861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485841
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999174
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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