A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138867



Internal ID21418454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27045652..27045652hg38UCSC Ensembl
chr4:27047274..27047274hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620039
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138867
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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