A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896764



Internal ID22671859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148155316..148159586hg38UCSC Ensembl
chr6:148476452..148480722hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg384271
hg194271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896764
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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