A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413135



Internal ID21070688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90307368..90310741hg38UCSC Ensembl
chr6:91017087..91020460hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383374
hg193374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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