A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688663



Internal ID21210520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:242162558..242163592hg38UCSC Ensembl
chr16:90284240..90285203hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381035
hg19964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2806210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688663
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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