A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153040



Internal ID15531125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:23495211..23571434hg38UCSC Ensembl
Innerchr5:23495320..23571543hg19UCSC Ensembl
Innerchr5:23531077..23607300hg18UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg3876224
hg1976224
hg1876224
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597544
Supporting Variants
SamplesHGDP01048
Known GenesPRDM9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153040
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