A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456200



Internal ID22514077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85577959..85594096hg38UCSC Ensembl
chr10:87337716..87353853hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3816138
hg1916138
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856197
Supporting Variants
Samples
Known GenesGRID1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456200
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