A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148742



Internal ID21489534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:30987199..30987288hg38UCSC Ensembl
chr6:30954976..30955065hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577238
Supporting Variants
SamplesNA18939
Known GenesMUC21
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148742
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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