A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757602



Internal ID20533462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141780984..141780984hg38UCSC Ensembl
chr7:141480784..141480784hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757602
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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