A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564781



Internal ID22433508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155482634..155482634hg38UCSC Ensembl
chr7:155275329..155275329hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338754
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564781
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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