A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519906



Internal ID18471501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34771494..34854419hg38UCSC Ensembl
Innerchr10:35060422..35143347hg19UCSC Ensembl
Innerchr10:35100428..35183353hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3882926
hg1982926
hg1882926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049119
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)nssv3519906
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