A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619495



Internal ID20992566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107924458..107934267hg38UCSC Ensembl
chr6:108245662..108255471hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg389810
hg199810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136966
Samples
Known GenesSEC63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619495
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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