A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1023783



Internal ID16317739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7169738..7200104hg38UCSC Ensembl
Innerchr5:7169851..7200217hg19UCSC Ensembl
Innerchr5:7222851..7253217hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3830367
hg1930367
hg1830367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596980
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1023783
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