A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027142



Internal ID21936485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9522711..9530032hg38UCSC Ensembl
chr17:9426028..9433349hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg387322
hg197322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631127
Samples
Known GenesSTX8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027142
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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