A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500064



Internal ID22558000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101996218..101997984hg38UCSC Ensembl
chr7:101639498..101641264hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381767
hg191767
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853445
Supporting Variants
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500064
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