A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407674



Internal ID22465544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11265150..11265150hg38UCSC Ensembl
chr2:11405276..11405276hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961652
Supporting Variants
Samples
Known GenesROCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407674
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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