A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137235



Internal ID21452190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55623713..55623713hg38UCSC Ensembl
chr4:56489880..56489880hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623147
Supporting Variants
SamplesHG01596
Known GenesNMU
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137235
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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