A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2559n100



Internal ID19012927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34403109..34578022hg38UCSC Ensembl
chr15:34695310..34870223hg19UCSC Ensembl
chr15:32482602..32657515hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38174914
hg19174914
hg18174914
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048728, nsv1054597, nsv1054353, nsv1037455, nsv1041644, nsv1035932, nsv1045615, nsv1045022, nsv1042726
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)dgv2559n100
Frequency
Sample Size29084
Observed Gain30
Observed Loss156
Observed Complex0
Frequencyn/a


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