A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033435



Internal ID21942778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124839695..124839775hg38UCSC Ensembl
chr12:125324241..125324321hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617442
Samples
Known GenesSCARB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033435
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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