A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910778



Internal ID22685989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168311559..168311662hg38UCSC Ensembl
chr6:168712239..168712342hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411254
Samples
Known GenesDACT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910778
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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