A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15207992



Internal ID5209808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33154927..33157644hg38UCSC Ensembl
Innerchr15:33154929..33157643hg38UCSC Ensembl
Outerchr15:33154926..33157646hg38UCSC Ensembl
chr15:33447128..33449845hg19UCSC Ensembl
Innerchr15:33447130..33449844hg19UCSC Ensembl
Outerchr15:33447127..33449847hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382718
hg192718
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636080
Supporting Variants
SamplesHG02667
Known GenesFMN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15207992
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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