A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048261



Internal ID18790792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32147032..32567645hg38UCSC Ensembl
Innerchr15:32439233..32859846hg19UCSC Ensembl
Innerchr15:30226525..30647138hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38420614
hg19420614
hg18420614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2538n100
Supporting Variantsnssv3547720
Samples
Known GenesCHRNA7, GOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048261
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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