A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607168



Internal ID20980239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135180701..135182200hg38UCSC Ensembl
chr6:135501839..135503338hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139472
Samples
Known GenesMYB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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