A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188342



Internal ID20755382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90322646..90846337hg38UCSC Ensembl
chr10:92082403..92606094hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38523692
hg19523692
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451156
Supporting Variants
Samples
Known GenesHTR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188342
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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