A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13722476



Internal ID5347634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25349345..25349925hg38UCSC Ensembl
Innerchr10:25349346..25349924hg38UCSC Ensembl
Outerchr10:25349344..25349926hg38UCSC Ensembl
chr10:25638274..25638854hg19UCSC Ensembl
Innerchr10:25638275..25638853hg19UCSC Ensembl
Outerchr10:25638273..25638855hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622665
Supporting Variants
SamplesNA18878
Known GenesGPR158
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13722476
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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