A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142903



Internal ID21414073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159980215..159980215hg38UCSC Ensembl
chr6:160401247..160401247hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639470
Supporting Variants
SamplesHG00513
Known GenesIGF2R
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142903
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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