A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174485



Internal ID20741525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102586583..102600827hg38UCSC Ensembl
chr9:105348865..105363109hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3814245
hg1914245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441929
Supporting Variants
Samples
Known GenesLINC00587
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174485
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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