A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577152



Internal ID21769195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75927807..75927807hg38UCSC Ensembl
chr6:76637524..76637524hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg384701
hg194701
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075806
Supporting Variants
Samples
Known GenesIMPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577152
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer