A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15230751



Internal ID5760550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42096891..42100177hg38UCSC Ensembl
Innerchr15:42096891..42100177hg38UCSC Ensembl
Outerchr15:42096628..42100436hg38UCSC Ensembl
chr15:42389089..42392375hg19UCSC Ensembl
Innerchr15:42389089..42392375hg19UCSC Ensembl
Outerchr15:42388826..42392634hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg383287
hg193287
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636256
Supporting Variants
SamplesNA19130
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15230751
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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