A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038405



Internal ID18780936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22385562..23199681hg38UCSC Ensembl
Innerchr15:22673387..23487534hg19UCSC Ensembl
Innerchr15:20224751..21038975hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38814120
hg19814148
hg18814225
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2407n100
Supporting Variantsnssv3538851, nssv3538853, nssv3538852
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)nsv1038405
Frequency
Sample Size29084
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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