A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636775



Internal ID21828822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5657666..5658101hg38UCSC Ensembl
chr17:5560986..5561421hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027992
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636775
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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