A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636252



Internal ID7023048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41920608..41930640hg38UCSC Ensembl
Innerchr15:41920619..41930629hg38UCSC Ensembl
Outerchr15:41920597..41930651hg38UCSC Ensembl
chr15:42212806..42222838hg19UCSC Ensembl
Innerchr15:42212817..42222827hg19UCSC Ensembl
Outerchr15:42212795..42222849hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3810033
hg1910033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15230587
SamplesHG01486
Known GenesEHD4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636252
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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