A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619658



Internal ID20992729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112101413..112103231hg38UCSC Ensembl
chr6:112422616..112424434hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381819
hg191819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135442
Samples
Known GenesFAM229B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619658
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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