A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997946



Internal ID20564987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13041801..13044200hg38UCSC Ensembl
chr12:13194735..13197134hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459336
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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