A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603400



Internal ID20976471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158541202..158552920hg38UCSC Ensembl
chr6:158962234..158973952hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3811719
hg1911719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141985
Samples
Known GenesTMEM181
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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