A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1023762



Internal ID16317718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6713146..6719051hg38UCSC Ensembl
Innerchr5:6713259..6719164hg19UCSC Ensembl
Innerchr5:6766259..6772164hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385906
hg195906
hg185906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596965
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)nssv1023762
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