A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406925



Internal ID21064478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92259432..92481599hg38UCSC Ensembl
chr6:92969150..93191317hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38222168
hg19222168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148710
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406925
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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