A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371946



Internal ID21029499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27250812..27276230hg38UCSC Ensembl
chr3:27292303..27317721hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3825419
hg1925419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101896
Samples
Known GenesNEK10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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