A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575751



Internal ID21767794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143814604..143814604hg38UCSC Ensembl
chr6:144135741..144135741hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6077977
Supporting Variants
Samples
Known GenesPHACTR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575751
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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