A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054646



Internal ID18797177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84153209..84546378hg38UCSC Ensembl
Innerchr15:84821961..85089609hg19UCSC Ensembl
Innerchr15:82612965..82890613hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38393170
hg19267649
hg18277649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2638n100
Supporting Variantsnssv3554644
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LOC100505679, LOC388152, LOC440300, LOC642423, UBE2Q2P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054646
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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