A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753938



Internal ID20529798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90315110..90315110hg38UCSC Ensembl
chr7:89944424..89944424hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg385931
hg195931
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753938
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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