A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041494



Internal ID18784025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438889..34563605hg38UCSC Ensembl
Innerchr15:34731090..34855806hg19UCSC Ensembl
Innerchr15:32518382..32643098hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38124717
hg19124717
hg18124717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2563n100
Supporting Variantsnssv3551676, nssv3551675
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041494
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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