A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037873



Internal ID18780404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32565269hg38UCSC Ensembl
Innerchr15:32458661..32857470hg19UCSC Ensembl
Innerchr15:30245953..30644762hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38398810
hg19398810
hg18398810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2538n100
Supporting Variantsnssv3547750, nssv3721618, nssv3547751, nssv3721617, nssv3547749, nssv3547748
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)nsv1037873
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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