A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834162



Internal ID22609097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97672411..97687865hg38UCSC Ensembl
chr2:98288874..98304328hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3815455
hg1915455
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489123, nssv17489124
Samples
Known GenesLINC01125
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834162
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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