A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695728



Internal ID15085694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:176878677..176880503hg38UCSC Ensembl
Innerchr5:176305678..176307504hg19UCSC Ensembl
Innerchr5:176238284..176240110hg18UCSC Ensembl
Innerchr5:176238284..176240110hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg381827
hg191827
hg181827
hg171827
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517492
Supporting Variants
Samples
Known GenesUNC5A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695728
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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