A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184458



Internal ID20751498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34923320..35284498hg38UCSC Ensembl
chr10:35212248..35573426hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38361179
hg19361179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438790
Supporting Variants
Samples
Known GenesCCNY, CREM, CUL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184458
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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