A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119685



Internal ID21414505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139726624..139726624hg38UCSC Ensembl
chr4:140647778..140647778hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38915
hg19915
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605743
Supporting Variants
SamplesHG00513
Known GenesMAML3, MGST2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119685
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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