A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649238



Internal ID21597543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28172264..28172264hg38UCSC Ensembl
chr17:26499290..26499290hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087670
SamplesHG03371
Known GenesNLK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649238
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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