A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3698786



Internal ID18650381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15642115..15707706hg38UCSC Ensembl
Innerchr1:15968610..16034201hg19UCSC Ensembl
Innerchr1:15841197..15906788hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3865592
hg1965592
hg1865592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006877
Supporting Variants
Samples
Known GenesDDI2, PLEKHM2, RSC1A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3698786
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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