A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896551



Internal ID22671645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158803561..158803660hg38UCSC Ensembl
chr6:159224593..159224692hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410141
Samples
Known GenesEZR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896551
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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