A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519634



Internal ID18471229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113499347..113757619hg38UCSC Ensembl
Innerchr10:115259106..115517378hg19UCSC Ensembl
Innerchr10:115249096..115507368hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38258273
hg19258273
hg18258273
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048819
Supporting Variants
Samples
Known GenesCASP7, HABP2, NRAP, PLEKHS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519634
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