A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361824



Internal ID22587493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11728633..11729030hg38UCSC Ensembl
chr12:11881567..11881964hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920378
Supporting Variants
Samples
Known GenesETV6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361824
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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