A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038144



Internal ID19127363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57349867..57486126hg38UCSC Ensembl
Innerchr15:57642065..57778324hg19UCSC Ensembl
Innerchr15:55429357..55565616hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38136260
hg19136260
hg18136260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2607n100
Supporting Variantsnssv3553589, nssv3553588
Samples
Known GenesCGNL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038144
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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