A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500897



Internal ID22558834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108345601..108356938hg38UCSC Ensembl
chr6:108666805..108678142hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3811338
hg1911338
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843985
Supporting Variants
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500897
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