A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3699598



Internal ID18651193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:86223405..86440219hg38UCSC Ensembl
Innerchr1:86689088..86905902hg19UCSC Ensembl
Innerchr1:86461676..86678490hg18UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38216815
hg19216815
hg18216815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002541
Supporting Variants
Samples
Known GenesCLCA2, MIR7856, ODF2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3699598
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