A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999529



Internal ID20566569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14480936..14481759hg38UCSC Ensembl
chr12:14633870..14634693hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470780
Supporting Variants
Samples
Known GenesATF7IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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