A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601384



Internal ID21793431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:123898863..123898863hg38UCSC Ensembl
chr12:124383410..124383410hg19UCSC 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 Variantsnsv6087303
Supporting Variants
Samples
Known GenesDNAH10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601384
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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