A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619579



Internal ID20992650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108083844..108090660hg38UCSC Ensembl
chr6:108405048..108411864hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386817
hg196817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136977
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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