A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190092



Internal ID20757132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37687801..37689000hg38UCSC Ensembl
chr9:37687798..37688997hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446376
Supporting Variants
Samples
Known GenesFRMPD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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