A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048688



Internal ID18791219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32565199hg38UCSC Ensembl
Innerchr15:32458661..32857400hg19UCSC Ensembl
Innerchr15:30245953..30644692hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38398740
hg19398740
hg18398740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2538n100
Supporting Variantsnssv3721616, nssv3547744, nssv3721615, nssv3547739, nssv3721614, nssv3547745, nssv3547736, nssv3547741, nssv3547747, nssv3547746, nssv3547737, nssv3547735, nssv3547742, nssv3547743, nssv3547740, nssv3721613, nssv3547738
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)nsv1048688
Frequency
Sample Size29084
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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