A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636301



Internal ID7023097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43945975..43954204hg38UCSC Ensembl
Innerchr15:43946025..43954154hg38UCSC Ensembl
Outerchr15:43945871..43954308hg38UCSC Ensembl
chr15:44238173..44246402hg19UCSC Ensembl
Innerchr15:44238223..44246352hg19UCSC Ensembl
Outerchr15:44238069..44246506hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg388230
hg198230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15231663
SamplesHG00592
Known GenesFRMD5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636301
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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