A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895588



Internal ID22670672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157178540..157178598hg38UCSC Ensembl
chr6:157499674..157499732hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410544
Samples
Known GenesARID1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895588
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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