A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366696



Internal ID22592365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106954096..106954145hg38UCSC Ensembl
chr12:107347874..107347923hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945330
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366696
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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