A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888870



Internal ID22663880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91670562..91672630hg38UCSC Ensembl
chr6:92380280..92382348hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg382069
hg192069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443116
Samples
Known GenesCASC6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888870
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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