A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042322



Internal ID18784853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1658508..1757404hg38UCSC Ensembl
Innerchr10:1700702..1799598hg19UCSC Ensembl
Innerchr10:1690702..1789598hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3898897
hg1998897
hg1898897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3486905
Samples
Known GenesADARB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042322
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