A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046628



Internal ID18789159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34408470..34522329hg38UCSC Ensembl
Innerchr15:34700671..34814530hg19UCSC Ensembl
Innerchr15:32487963..32601822hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38113860
hg19113860
hg18113860
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2558n100
Supporting Variantsnssv3548868, nssv3548875, nssv3548867, nssv3721740, nssv3548870, nssv3548869, nssv3548871, nssv3721746, nssv3548878, nssv3721742, nssv3721741, nssv3548877, nssv3721745, nssv3548872, nssv3721747, nssv3548876, nssv3721743, nssv3548874, nssv3721744, nssv3548873
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046628
Frequency
Sample Size29084
Observed Gain2
Observed Loss18
Observed Complex0
Frequencyn/a


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