A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052699



Internal ID19141918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..21997806hg38UCSC Ensembl
Innerchr15:20585976..22285757hg19UCSC Ensembl
Innerchr15:18845990..19787121hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381617084
hg191699782
hg18941132
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2250n100
Supporting Variantsnssv3537339, nssv3537317, nssv3537334, nssv3714666, nssv3537342, nssv3537337, nssv3714667, nssv3537327, nssv3537324, nssv3714665, nssv3537330, nssv3537328, nssv3537336, nssv3537341, nssv3537321, nssv3537333, nssv3537322, nssv3714664, nssv3537331, nssv3537343, nssv3537318, nssv3537320, nssv3537338, nssv3537319, nssv3537335, nssv3537332, nssv3537340, nssv3537326, nssv3537316, nssv3537329, nssv3537325, nssv3537344, nssv3537323
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, 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)nsv1052699
Frequency
Sample Size11257
Observed Gain12
Observed Loss21
Observed Complex0
Frequencyn/a


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