A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637213



Internal ID21585518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29200843..29200843hg38UCSC Ensembl
chr9:29200841..29200841hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161576
SamplesHG01114
Known GenesLINGO2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637213
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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