A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768003



Internal ID20543863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66989258..66989258hg38UCSC Ensembl
chr7:66454245..66454245hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279818
Samples
Known GenesSBDS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768003
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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