A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923754



Internal ID22698981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29162105..29163207hg38UCSC Ensembl
chr12:29315038..29316140hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg381103
hg191103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17349881
Samples
Known GenesFAR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923754
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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