A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010839



Internal ID18753372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:177913037..177958519hg38UCSC Ensembl
Innerchr1:177882172..177927654hg19UCSC Ensembl
Innerchr1:176148795..176194277hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3845483
hg1945483
hg1845483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3499073, nssv3498097, nssv3704828
Samples
Known GenesSEC16B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010839
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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