A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038902



Internal ID18781433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30338750..30487481hg38UCSC Ensembl
Innerchr15:30630953..30779684hg19UCSC Ensembl
Innerchr15:28418245..28566976hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38148732
hg19148732
hg18148732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2521n100
Supporting Variantsnssv3546775
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038902
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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