A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747378



Internal ID15694648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46166132..46331115hg38UCSC Ensembl
Innerchr10:47537368..47702351hg19UCSC Ensembl
Innerchr10:47007374..47172357hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38164984
hg19164984
hg18164984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550733
Supporting Variants
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747378
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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