A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8969313



Internal ID13818872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85681718..85681730hg38UCSC Ensembl
Innerchr15:85681709..85681736hg38UCSC Ensembl
Outerchr15:85681697..85681751hg38UCSC Ensembl
chr15:86224949..86224961hg19UCSC Ensembl
Innerchr15:86224940..86224967hg19UCSC Ensembl
Outerchr15:86224928..86224982hg19UCSC Ensembl
chr15:84025953..84025965hg18UCSC Ensembl
Innerchr15:84025971..84025944hg18UCSC Ensembl
Outerchr15:84025932..84025986hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38260
hg19260
hg18260
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3405577
Supporting Variants
SamplesNA18505
Known GenesAKAP13
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8969313
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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