A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527305



Internal ID20900666
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 StatusM
Merged Variants
Supporting Variantsnssv18203261
Samples
Known GenesDUSP15, FOXS1, MYLK2, PDRG1, TPX2, TTLL9, XKR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527305
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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