A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152247



Internal ID21460355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24417779..24417779hg38UCSC Ensembl
chr6:24418007..24418007hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631554
Supporting Variants
SamplesHG02818
Known GenesMRS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152247
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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