A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853032



Internal ID22627967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14761621..14763020hg38UCSC Ensembl
chr12:14914555..14915954hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457107, nssv17469567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853032
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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