A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598445



Internal ID21790490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124428044..124428044hg38UCSC Ensembl
chr12:124912590..124912590hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084479
Supporting Variants
Samples
Known GenesNCOR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598445
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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