A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263052



Internal ID20472270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6267530..6267602hg38UCSC Ensembl
chr17:6170850..6170922hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263052
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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