A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853831



Internal ID22628766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96340103..96342378hg38UCSC Ensembl
chr12:96733881..96736156hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg382276
hg192276
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469468
Samples
Known GenesCDK17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853831
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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