A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609685



Internal ID21801732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16573576..16573576hg38UCSC Ensembl
chr12:16726510..16726510hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg381585
hg191585
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080794
Supporting Variants
Samples
Known GenesLMO3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609685
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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