A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046264



Internal ID18788795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30158154..30529543hg38UCSC Ensembl
Innerchr15:30450357..30821746hg19UCSC Ensembl
Innerchr15:28237649..28609038hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38371390
hg19371390
hg18371390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2499n100
Supporting Variantsnssv3546553, nssv3546549, nssv3721511, nssv3721512, nssv3546552, nssv3546551, nssv3546550, nssv3546554
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)nsv1046264
Frequency
Sample Size29084
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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