A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071361



Internal ID21471430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86865229..86865229hg38UCSC Ensembl
chr10:88624986..88624986hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644438
Supporting Variants
SamplesHG03125
Known GenesBMPR1A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071361
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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