A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153035



Internal ID15532845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10236924..10262046hg38UCSC Ensembl
Innerchr5:10237036..10262158hg19UCSC Ensembl
Innerchr5:10290036..10315158hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3825123
hg1925123
hg1825123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597112
Supporting Variants
SamplesHGDP01383
Known GenesCCT5, FAM173B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153035
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