A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352036



Internal ID22577705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50782455..50794149hg38UCSC Ensembl
chr12:51176238..51187932hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3811695
hg1911695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938783
Supporting Variants
Samples
Known GenesATF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352036
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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