A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759730



Internal ID20535590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139101415..139101415hg38UCSC Ensembl
chr7:138786161..138786161hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259949
Samples
Known GenesZC3HAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759730
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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