A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054597



Internal ID18797128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34421910..34563605hg38UCSC Ensembl
Innerchr15:34714111..34855806hg19UCSC Ensembl
Innerchr15:32501403..32643098hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38141696
hg19141696
hg18141696
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2559n100
Supporting Variantsnssv3548927, nssv3721775, nssv3548925, nssv3548926
Samples
Known GenesGOLGA8A, GOLGA8B, 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)nsv1054597
Frequency
Sample Size29084
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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