A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154632



Internal ID21504107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118970008..118970008hg38UCSC Ensembl
chr6:119291173..119291173hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642839
Supporting Variants
SamplesNA19239
Known GenesFAM184A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154632
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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