A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649604



Internal ID21597909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76073501..76073501hg38UCSC Ensembl
chr17:74069582..74069582hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg383414
hg193414
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091617
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649604
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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