A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356027



Internal ID21013580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:12945147..12948851hg38UCSC Ensembl
chr3:12986647..12990351hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg383705
hg193705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093224
Samples
Known GenesIQSEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356027
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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