A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605091



Internal ID20978162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138829901..138838884hg38UCSC Ensembl
chr6:139151038..139160021hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg388984
hg198984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138406
Samples
Known GenesECT2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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