A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638901



Internal ID21587206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150372324..150372324hg38UCSC Ensembl
chr6:150693460..150693460hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147731
SamplesNA19239
Known GenesIYD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638901
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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