A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148323



Internal ID21503844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38699842..38699891hg38UCSC Ensembl
chr6:38667618..38667667hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571596
Supporting Variants
SamplesNA19239
Known GenesGLO1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148323
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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