A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053201



Internal ID19142420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..21997806hg38UCSC Ensembl
Innerchr15:20284054..22285757hg19UCSC Ensembl
Innerchr15:18544068..19787121hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381919006
hg192001704
hg181243054
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2190n100
Supporting Variantsnssv3536600, nssv3536591, nssv3536595, nssv3715992, nssv3536607, nssv3536605, nssv3536606, nssv3536588, nssv3536593, nssv3715994, nssv3536598, nssv3536599, nssv3536602, nssv3536604, nssv3715993, nssv3536597, nssv3715995, nssv3536603, nssv3536590, nssv3536594, nssv3536589, nssv3536592, nssv3536601, nssv3715991, nssv3536596
Samples
Known GenesCHEK2P2, CT60, 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)nsv1053201
Frequency
Sample Size11257
Observed Gain22
Observed Loss3
Observed Complex0
Frequencyn/a


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