A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410525



Internal ID21068078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46824805..46837278hg38UCSC Ensembl
chr6:46792542..46805015hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3812474
hg1912474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144250
Samples
Known GenesMEP1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410525
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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