A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901571



Internal ID22676722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156908793..156920561hg38UCSC Ensembl
chr6:157229927..157241695hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3811769
hg1911769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421155
Samples
Known GenesARID1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901571
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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