A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039729



Internal ID19128948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..21078935hg38UCSC Ensembl
Innerchr15:20585976..21284264hg19UCSC Ensembl
Innerchr15:18845990..19548923hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38698213
hg19698289
hg18702934
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2246n100
Supporting Variantsnssv3537293, nssv3714657, nssv3537292, nssv3537296, nssv3537294, nssv3537295, nssv3714656, nssv3537297
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, 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)nsv1039729
Frequency
Sample Size11257
Observed Gain5
Observed Loss3
Observed Complex0
Frequencyn/a


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