A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002698



Internal ID18745230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:167791252..167864873hg38UCSC Ensembl
Innerchr1:167760489..167834111hg19UCSC Ensembl
Innerchr1:166027113..166100735hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3873622
hg1973623
hg1873623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3704813
Samples
Known GenesADCY10, MPZL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002698
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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