A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035318



Internal ID18777849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20868184..21997806hg38UCSC Ensembl
Innerchr15:21073513..22285757hg19UCSC Ensembl
Innerchr15:19338171..19787121hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381129623
hg191212245
hg18448951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2347n100
Supporting Variantsnssv3541347
Samples
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035318
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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