A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614982



Internal ID20988053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143285794..143290130hg38UCSC Ensembl
chr6:143606931..143611267hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg384337
hg194337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140221
Samples
Known GenesAIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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