A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358976



Internal ID22584645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27062340..27062464hg38UCSC Ensembl
chr12:27215273..27215397hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925686
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358976
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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