A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2613n100



Internal ID22788700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61061570..61077286hg38UCSC Ensembl
chr15:61353769..61369485hg19UCSC Ensembl
chr15:59141061..59156777hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3815717
hg1915717
hg1815717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041307, nsv1038127
Samples
Known GenesRORA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2613n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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