A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367257



Internal ID22592926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103460839..103460979hg38UCSC Ensembl
chr1:104003461..104003601hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881777
Supporting Variants
Samples
Known GenesLOC101928436
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367257
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer