A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414369



Internal ID21071922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33995561..34001368hg38UCSC Ensembl
chr6:33963338..33969145hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg385808
hg195808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142873
Samples
Known GenesMIR1275
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414369
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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