A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100169



Internal ID22009402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8608257..8608257hg38UCSC Ensembl
chr12:8760853..8760853hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609903
Samples
Known GenesAICDA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100169
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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