A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635730



Internal ID21584035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75924756..75924756hg38UCSC Ensembl
chr6:76634473..76634473hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147310
SamplesHG00731
Known GenesIMPG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635730
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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