A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095571



Internal ID22004804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50135276..50135276hg38UCSC Ensembl
chr12:50529059..50529059hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598729
Samples
Known GenesCERS5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095571
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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