A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900955



Internal ID22676102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31268646..31353767hg38UCSC Ensembl
chr6:31236423..31321544hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3885122
hg1985122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1753n209
Supporting Variantsnssv17442043
Samples
Known GenesHLA-C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900955
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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