A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203261



Internal ID20770301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31763891..31974354hg38UCSC Ensembl
chr20:30351694..30562157hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38210464
hg19210464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527305
Supporting Variants
Samples
Known GenesDUSP15, FOXS1, MYLK2, PDRG1, TPX2, TTLL9, XKR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203261
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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