A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100155



Internal ID22009388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6504186..6504186hg38UCSC Ensembl
chr12:6613352..6613352hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612096
Samples
Known GenesNCAPD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100155
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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