A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8651923



Internal ID15100625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40050418..40051041hg38UCSC Ensembl
Innerchr15:40050418..40051041hg38UCSC Ensembl
Outerchr15:40049263..40051731hg38UCSC Ensembl
chr15:40342619..40343242hg19UCSC Ensembl
Innerchr15:40342619..40343242hg19UCSC Ensembl
Outerchr15:40341464..40343932hg19UCSC Ensembl
chr15:38129911..38130534hg18UCSC Ensembl
Innerchr15:38129911..38130534hg18UCSC Ensembl
Outerchr15:38128756..38131224hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38624
hg19624
hg18624
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3334538
Supporting Variants
SamplesNA19240
Known GenesSRP14-AS1
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8651923
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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