A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832932



Internal ID22607867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27587854..27588953hg38UCSC Ensembl
chr2:27810721..27811820hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484082
Samples
Known GenesZNF512
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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