A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270624



Internal ID20479842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17691311..17691395hg38UCSC Ensembl
chr2:17872578..17872662hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747480
Supporting Variants
Samples
Known GenesSMC6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270624
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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