A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865836



Internal ID22640771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14499787..14529533hg38UCSC Ensembl
chr12:14652721..14682467hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg3829747
hg1929747
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455954
Samples
Known GenesATF7IP, PLBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865836
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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