A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636632



Internal ID21584937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20619165..20619165hg38UCSC Ensembl
chr7:20658788..20658788hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142574
SamplesHG01505
Known GenesABCB5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636632
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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