A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174508



Internal ID15533648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46224041..46279254hg38UCSC Ensembl
Innerchr10:47595277..47650490hg19UCSC Ensembl
Innerchr10:47065283..47120496hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3855214
hg1955214
hg1855214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550775
Supporting Variants
SamplesNINDS_197
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174508
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