A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856790



Internal ID22631725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50783140..50795522hg38UCSC Ensembl
chr12:51176923..51189305hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3812383
hg1912383
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454040, nssv17454944
Samples
Known GenesATF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856790
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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