A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3361212



Internal ID15208190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36659626..36659642hg38UCSC Ensembl
Innerchr15:36659628..36659640hg38UCSC Ensembl
Outerchr15:36659624..36659644hg38UCSC Ensembl
chr15:36951827..36951843hg19UCSC Ensembl
Innerchr15:36951829..36951841hg19UCSC Ensembl
Outerchr15:36951825..36951845hg19UCSC Ensembl
chr15:34739119..34739135hg18UCSC Ensembl
Innerchr15:34739121..34739133hg18UCSC Ensembl
Outerchr15:34739117..34739137hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865802
SamplesNA12005
Known GenesC15orf41
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3361212
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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