A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036631



Internal ID18779162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30201146..30515727hg38UCSC Ensembl
Innerchr15:30493349..30807930hg19UCSC Ensembl
Innerchr15:28280641..28595222hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38314582
hg19314582
hg18314582
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2502n100
Supporting Variantsnssv3721517, nssv3721518, nssv3546577, nssv3546576, nssv3546575
Samples
Known GenesCHRFAM7A, DKFZP434L187, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036631
Frequency
Sample Size29084
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


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