A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405025



Internal ID21062578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85834901..85861700hg38UCSC Ensembl
chr6:86544619..86571418hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3826800
hg1926800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6301n223
Supporting Variantsnssv18146080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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