A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751788



Internal ID20527648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103178120..103178120hg38UCSC Ensembl
chr7:102818567..102818567hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285598
Samples
Known GenesDPY19L2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751788
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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