A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863265



Internal ID22638200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29861808..29869552hg38UCSC Ensembl
chr12:30014741..30022485hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg387745
hg197745
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458661, nssv17458274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863265
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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