A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045697



Internal ID19134916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..22308242hg38UCSC Ensembl
Innerchr15:20585976..22673387hg19UCSC Ensembl
Innerchr15:18845990..20224751hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381927520
hg192087412
hg181378762
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2193n100
Supporting Variantsnssv3537504, nssv3537503, nssv3537493, nssv3537497, nssv3537500, nssv3537495, nssv3537490, nssv3537491, nssv3537499, nssv3537496, nssv3537498, nssv3714716, nssv3714714, nssv3537502, nssv3537501, nssv3714715, nssv3537489, nssv3537505, nssv3537492, nssv3537494
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045697
Frequency
Sample Size11257
Observed Gain3
Observed Loss17
Observed Complex0
Frequencyn/a


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