A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285166



Internal ID20494384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168537230..168537307hg38UCSC Ensembl
chr6:168937910..168937987hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747840
Supporting Variants
Samples
Known GenesSMOC2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285166
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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