A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407386



Internal ID21064939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15149826..15160135hg38UCSC Ensembl
chr6:15150057..15160366hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3810310
hg1910310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6064n223
Supporting Variantsnssv18141500
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407386
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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