A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610691



Internal ID20983762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143439843..143442010hg38UCSC Ensembl
chr6:143760980..143763147hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg382168
hg192168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140232
Samples
Known GenesADAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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