A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151004



Internal ID21489449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119289433..119289532hg38UCSC Ensembl
chr6:119610598..119610697hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577071
Supporting Variants
SamplesNA18939
Known GenesMAN1A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151004
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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