A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044337



Internal ID18786868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101182262..101351332hg38UCSC Ensembl
Innerchr15:101722467..101891537hg19UCSC Ensembl
Innerchr15:99539990..99709060hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38169071
hg19169071
hg18169071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2673n100
Supporting Variantsnssv3555335
Samples
Known GenesCHSY1, LOC100507472, PCSK6, SNRPA1, VIMP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044337
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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