A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998881



Internal ID20565921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2985823..2986512hg38UCSC Ensembl
chr12:3094989..3095678hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460374
Supporting Variants
Samples
Known GenesTEAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998881
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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