A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15305126



Internal ID5108977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80102339..80115096hg38UCSC Ensembl
Innerchr15:80102340..80115095hg38UCSC Ensembl
Outerchr15:80102338..80115097hg38UCSC Ensembl
chr15:80394681..80407438hg19UCSC Ensembl
Innerchr15:80394682..80407437hg19UCSC Ensembl
Outerchr15:80394680..80407439hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3812758
hg1912758
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637013
Supporting Variants
SamplesNA18558
Known GenesZFAND6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15305126
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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