A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171655



Internal ID20738695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101666588..101667130hg38UCSC Ensembl
chr9:104428870..104429412hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453592
Supporting Variants
Samples
Known GenesGRIN3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0004


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