A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132528



Internal ID21510231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139314998..139314998hg38UCSC Ensembl
chr4:140236152..140236152hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623033
Supporting Variants
SamplesNA24385
Known GenesNAA15
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132528
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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