A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356143



Internal ID21013696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25860026..25861443hg38UCSC Ensembl
chr3:25901517..25902934hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381418
hg191418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101146
Samples
Known GenesLINC00692
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356143
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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