A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579641



Internal ID21528122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66382950..66383254hg38UCSC Ensembl
chr7:65847937..65848241hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158519
SamplesHG03065
Known GenesLINC00174
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579641
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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