A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997533



Internal ID20564573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12844001..12870740hg38UCSC Ensembl
chr12:12996935..13023674hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg3826740
hg1926740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467909
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997533
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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