A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357630



Internal ID22583299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96434080..96435805hg38UCSC Ensembl
chr12:96827858..96829583hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381726
hg191726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936838
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357630
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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