A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006660



Internal ID19095877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:53291070..53381136hg38UCSC Ensembl
Innerchr1:53756742..53846808hg19UCSC Ensembl
Innerchr1:53529330..53619396hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3890067
hg1990067
hg1890067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv165n100
Supporting Variantsnssv3469356
Samples
Known GenesLRP8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006660
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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