A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568922



Internal ID21517274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97939146..97939329hg38UCSC Ensembl
chr7:97568458..97568641hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141687
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568922
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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