A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410885



Internal ID21068438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91450762..91484407hg38UCSC Ensembl
chr6:92160480..92194125hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3833646
hg1933646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6310n223
Supporting Variantsnssv18145488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410885
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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