A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408488



Internal ID21066041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72138205..72167296hg38UCSC Ensembl
chr6:72847908..72876999hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3829092
hg1929092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147385
Samples
Known GenesRIMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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