A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637721



Internal ID21586026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48923506..48923506hg38UCSC Ensembl
chr10:50131551..50131551hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070612
SamplesHG00731
Known GenesWDFY4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637721
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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