A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636080



Internal ID6676189
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15207992
SamplesHG02667
Known GenesFMN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636080
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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