A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1023778



Internal ID15971048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6713819..6715972hg38UCSC Ensembl
Innerchr5:6713932..6716085hg19UCSC Ensembl
Innerchr5:6766932..6769085hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg382154
hg192154
hg182154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596975
Supporting Variants
Samples
Known GenesPAPD7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1023778
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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