A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051299



Internal ID18793830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22413906..23199681hg38UCSC Ensembl
Innerchr15:22673387..23459190hg19UCSC Ensembl
Innerchr15:20224751..21010631hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38785776
hg19785804
hg18785881
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2407n100
Supporting Variantsnssv3538849, nssv3538846, nssv3538845, nssv3538847, nssv3715530, nssv3715529, nssv3538848
Samples
Known GenesCYFIP1, GOLGA6L1, GOLGA8DP, GOLGA8EP, GOLGA8I, HERC2P2, HERC2P7, LOC283683, MIR4509-1, MIR4509-2, MIR4509-3, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051299
Frequency
Sample Size29084
Observed Gain2
Observed Loss5
Observed Complex0
Frequencyn/a


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