A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610098



Internal ID20983169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158454605..158459597hg38UCSC Ensembl
chr6:158875637..158880629hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384993
hg194993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141981
Samples
Known GenesTULP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610098
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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