A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037732



Internal ID19126951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84153209..84402534hg38UCSC Ensembl
Innerchr15:84821961..84957232hg19UCSC Ensembl
Innerchr15:82612965..82748236hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38249326
hg19135272
hg18135272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2639n100
Supporting Variantsnssv3554635, nssv3554637, nssv3554638, nssv3554633, nssv3554636, nssv3554634
Samples
Known GenesDNM1P41, GOLGA6L4, LOC100505679, LOC388152, LOC440300, LOC642423
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037732
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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