A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014588



Internal ID19103806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:160428550..160451870hg38UCSC Ensembl
Innerchr1:160398340..160421660hg19UCSC Ensembl
Innerchr1:158664964..158688284hg18UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3823321
hg1923321
hg1823321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3704746
Samples
Known GenesVANGL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014588
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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