A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647677



Internal ID21595982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81307349..81307349hg38UCSC Ensembl
chr17:79281149..79281149hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094431
SamplesHG03009
Known GenesLINC00482
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647677
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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