A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151600



Internal ID21405217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87576043..87576518hg38UCSC Ensembl
chr6:88285761..88286236hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582147
Supporting Variants
SamplesHG00512
Known GenesRARS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151600
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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