A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673387



Internal ID15410039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166789500..166797813hg38UCSC Ensembl
Innerchr1:166758737..166767050hg19UCSC Ensembl
Innerchr1:165025361..165033674hg18UCSC Ensembl
Innerchr1:163490395..163498708hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg388314
hg198314
hg188314
hg178314
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519275
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673387
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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