A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634014



Internal ID21582319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72043662..72043662hg38UCSC Ensembl
chr6:72753365..72753365hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144310
SamplesNA19238
Known GenesRIMS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634014
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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