A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649704



Internal ID21598009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65620716..65620716hg38UCSC Ensembl
chr17:63616834..63616834hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095132
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649704
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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