A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501181



Internal ID22559118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12547493..12589231hg38UCSC Ensembl
chr7:12587119..12628856hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3841739
hg1941738
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846403
Supporting Variants
Samples
Known GenesSCIN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501181
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