A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627850



Internal ID21819897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30497099..30507087hg38UCSC Ensembl
chr17:28824117..28834105hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg389989
hg199989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036065
Supporting Variants
Samples
Known GenesGOSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627850
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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