A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102906



Internal ID20669946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57624321..57629601hg38UCSC Ensembl
chr3:57610048..57615328hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg385281
hg195281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358275
Supporting Variants
Samples
Known GenesDENND6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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