A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888409



Internal ID22663415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77885013..77885388hg38UCSC Ensembl
chr6:78594730..78595105hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448246
Samples
Known GenesMEI4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888409
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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