A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144061



Internal ID21496332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6537575..6537575hg38UCSC Ensembl
chr6:6537808..6537808hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632206
Supporting Variants
SamplesNA19238
Known GenesLY86-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144061
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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