A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051027



Internal ID19140246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57354934..57474321hg38UCSC Ensembl
Innerchr15:57647132..57766519hg19UCSC Ensembl
Innerchr15:55434424..55553811hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38119388
hg19119388
hg18119388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2607n100
Supporting Variantsnssv3553605
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)nsv1051027
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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