A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621563



Internal ID21569868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202256893..202256893hg38UCSC Ensembl
chr1:202226021..202226021hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg383410
hg193410
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062092
SamplesHG02587
Known GenesLGR6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621563
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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