A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862947



Internal ID22637882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50810558..50823129hg38UCSC Ensembl
chr12:51204341..51216912hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3812572
hg1912572
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454937
Samples
Known GenesATF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862947
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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