A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038778



Internal ID18781309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50904444..51064531hg38UCSC Ensembl
Innerchr15:51196641..51356728hg19UCSC Ensembl
Innerchr15:48983933..49144020hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38160088
hg19160088
hg18160088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552398
Samples
Known GenesAP4E1, DCAF13P3, TNFAIP8L3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038778
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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