A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520384



Internal ID18818665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82503688..82574754hg38UCSC Ensembl
Innerchr10:84263444..84334510hg19UCSC Ensembl
Innerchr10:84253424..84324490hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3871067
hg1971067
hg1871067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051317
Supporting Variants
Samples
Known GenesNRG3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3520384
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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