A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607119



Internal ID20980190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116137246..116138493hg38UCSC Ensembl
chr6:116458409..116459656hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg381248
hg191248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137125
Samples
Known GenesNT5DC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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