A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583435



Internal ID21775478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133657414..133657478hg38UCSC Ensembl
chr9:136522536..136522600hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002072
Supporting Variants
Samples
Known GenesDBH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583435
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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