A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636236



Internal ID7023032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41171721..41172925hg38UCSC Ensembl
Innerchr15:41171771..41172875hg38UCSC Ensembl
Outerchr15:41171671..41172975hg38UCSC Ensembl
chr15:41463919..41465123hg19UCSC Ensembl
Innerchr15:41463969..41465073hg19UCSC Ensembl
Outerchr15:41463869..41465173hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381205
hg191205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15230035, essv15230039, essv15230036, essv15230038, essv15230037
SamplesHG04195, NA20126, NA19225, HG03162, HG02808
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636236
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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