A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071072



Internal ID21980305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169209682..169209682hg38UCSC Ensembl
chr4:170130833..170130833hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540798
Samples
Known GenesSH3RF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071072
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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