A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951261



Internal ID21371330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155954589..155954589hg38UCSC Ensembl
chr1:155924380..155924380hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187049
SamplesHG002
Known GenesARHGEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951261
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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