A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699008



Internal ID15435660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59679436..59681364hg38UCSC Ensembl
Innerchr15:59971635..59973563hg19UCSC Ensembl
Innerchr15:57758927..57760855hg18UCSC Ensembl
Innerchr15:57758927..57760855hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381929
hg191929
hg181929
hg171929
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523274
Supporting Variants
Samples
Known GenesBNIP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699008
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