A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055055



Internal ID18797586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89683716..89733369hg38UCSC Ensembl
Innerchr15:90226947..90276600hg19UCSC Ensembl
Innerchr15:88027951..88077604hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3849654
hg1949654
hg1849654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555195
Samples
Known GenesPEX11A, WDR93
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055055
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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