A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510385



Internal ID18461980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34697315..34898649hg38UCSC Ensembl
Innerchr10:34986243..35187577hg19UCSC Ensembl
Innerchr10:35026249..35227583hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38201335
hg19201335
hg18201335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038748
Supporting Variants
Samples
Known GenesPARD3, PARD3-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3510385
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