A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2637n100



Internal ID20154253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82568764..82803755hg38UCSC Ensembl
chr15:83237514..83472507hg19UCSC Ensembl
chr15:81034569..81269561hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38234992
hg19234994
hg18234993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036462, nsv1054171, nsv1036950
Samples
Known GenesAP3B2, CPEB1, FSD2, LOC283692, LOC283693, LOC338963, SCARNA15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2637n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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