A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767499



Internal ID20543359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128107571..128107571hg38UCSC Ensembl
chr7:127747623..127747623hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767499
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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