A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610597



Internal ID21802644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25520489..25529613hg38UCSC Ensembl
chr12:25673423..25682547hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg389125
hg199125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026277
Supporting Variants
Samples
Known GenesIFLTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610597
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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