A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364225



Internal ID21021778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:12090501..12093500hg38UCSC Ensembl
chr3:12132001..12135000hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093612
Samples
Known GenesSYN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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