A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149257



Internal ID21457017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90367231..90367290hg38UCSC Ensembl
chr6:91076950..91077009hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573640
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149257
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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