A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625949



Internal ID21574254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35906568..35906568hg38UCSC Ensembl
chr9:35906565..35906565hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161723
SamplesHG00732
Known GenesHRCT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625949
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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