A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335136



Internal ID20868327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220643614..220648515hg38UCSC Ensembl
chr1:220816956..220821857hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg384902
hg194902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058470
Samples
Known GenesMARK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335136
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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