A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15271568



Internal ID3060190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64268374..64274826hg38UCSC Ensembl
Innerchr15:64268379..64274821hg38UCSC Ensembl
Outerchr15:64268369..64274831hg38UCSC Ensembl
chr15:64560573..64567025hg19UCSC Ensembl
Innerchr15:64560578..64567020hg19UCSC Ensembl
Outerchr15:64560568..64567030hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg386453
hg196453
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636731
Supporting Variants
SamplesHG02688
Known GenesCSNK1G1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15271568
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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