A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2623n100



Internal ID22788710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76139033..76198206hg38UCSC Ensembl
chr15:76431374..76490547hg19UCSC Ensembl
chr15:74218429..74277602hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3859174
hg1959174
hg1859174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045860, nsv1039595, nsv1047539, nsv1042750, nsv1036319, nsv1054289, nsv1053643, nsv1052496, nsv1035806
Samples
Known GenesC15orf27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2623n100
Frequency
Sample Size11257
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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