A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762929



Internal ID20538789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7331221..7331221hg38UCSC Ensembl
chr11:7352452..7352452hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288643
Samples
Known GenesSYT9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762929
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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