A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617176



Internal ID20990247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102883708..102889726hg38UCSC Ensembl
chr6:103331583..103337601hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135875
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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