A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15333886



Internal ID2692822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97877569..97878712hg38UCSC Ensembl
Innerchr15:97877569..97878712hg38UCSC Ensembl
Outerchr15:97877384..97878933hg38UCSC Ensembl
chr15:98420799..98421942hg19UCSC Ensembl
Innerchr15:98420799..98421942hg19UCSC Ensembl
Outerchr15:98420614..98422163hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381144
hg191144
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637387
Supporting Variants
SamplesHG02383
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15333886
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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