A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636481



Internal ID21584786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:8152704..8152704hg38UCSC Ensembl
chr7:8192334..8192334hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140921
SamplesHG00732
Known GenesICA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636481
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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