A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399031



Internal ID21056584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15146133..15158525hg38UCSC Ensembl
chr6:15146364..15158756hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3812393
hg1912393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6064n223
Supporting Variantsnssv18141495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399031
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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