A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474344



Internal ID22532238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88646005..88653393hg38UCSC Ensembl
chr15:89189236..89196624hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg387389
hg197389
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868981
Supporting Variants
Samples
Known GenesISG20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474344
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