A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616240



Internal ID20989311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155144279..155174644hg38UCSC Ensembl
chr6:155465413..155495778hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3830366
hg1930366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139771
Samples
Known GenesTIAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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