A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043100



Internal ID19132319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20217113..22300068hg38UCSC Ensembl
Innerchr15:20422366..22588019hg19UCSC Ensembl
Innerchr15:18682380..20089383hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382082956
hg192165654
hg181407004
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2191n100
Supporting Variantsnssv3539380, nssv3716534, nssv3539383, nssv3716531, nssv3539391, nssv3539385, nssv3539386, nssv3539392, nssv3539381, nssv3539388, nssv3716530, nssv3539379, nssv3539384, nssv3716529, nssv3716532, nssv3539387, nssv3539390, nssv3539389, nssv3539382, nssv3716533
Samples
Known GenesCHEK2P2, CT60, 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)nsv1043100
Frequency
Sample Size11257
Observed Gain13
Observed Loss7
Observed Complex0
Frequencyn/a


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