A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264936



Internal ID20474154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55871365..55871365hg38UCSC Ensembl
chr12:56265149..56265149hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264936
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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