A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855760



Internal ID22630695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66300377..66310631hg38UCSC Ensembl
chr7:65765364..65775618hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3810255
hg1910255
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501478
Samples
Known GenesTPST1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855760
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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