A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039677



Internal ID18782208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30628409..30807411hg38UCSC Ensembl
Innerchr15:30920612..31099614hg19UCSC Ensembl
Innerchr15:28707904..28886906hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38179003
hg19179003
hg18179003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2533n100
Supporting Variantsnssv3547641
Samples
Known GenesARHGAP11B, LOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039677
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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