A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195197



Internal ID20762237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42100701..42265400hg38UCSC Ensembl
chr10:42596688..42760848hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38164700
hg19164161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442894
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195197
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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