A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232314



Internal ID20799354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89376654..90197092hg38UCSC Ensembl
chr6:90086373..90906811hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38820439
hg19820439
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405432
Supporting Variants
Samples
Known GenesANKRD6, BACH2, CASP8AP2, GJA10, LYRM2, MDN1, RRAGD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232314
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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