A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053477



Internal ID18796008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30212863..30515727hg38UCSC Ensembl
Innerchr15:30505066..30807930hg19UCSC Ensembl
Innerchr15:28292358..28595222hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38302865
hg19302865
hg18302865
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2502n100
Supporting Variantsnssv3546655, nssv3546656, nssv3546657
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)nsv1053477
Frequency
Sample Size29084
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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