A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180604



Internal ID20747644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34881089..35029485hg38UCSC Ensembl
chr10:35170017..35318413hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38148397
hg19148397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435707
Supporting Variants
Samples
Known GenesCUL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180604
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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