A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041644



Internal ID18784175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34570046hg38UCSC Ensembl
Innerchr15:34695310..34862247hg19UCSC Ensembl
Innerchr15:32482602..32649539hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38166938
hg19166938
hg18166938
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2559n100
Supporting Variantsnssv3548797, nssv3548799, nssv3548798
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)nsv1041644
Frequency
Sample Size29084
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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