A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656759



Internal ID21605064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59569700..59569700hg38UCSC Ensembl
chr17:57647061..57647061hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085922
SamplesNA19238
Known GenesDHX40
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656759
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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