A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13664645



Internal ID1707155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:752781..774643hg38UCSC Ensembl
Innerchr10:752781..774643hg38UCSC Ensembl
Outerchr10:752281..775143hg38UCSC Ensembl
chr10:798721..820583hg19UCSC Ensembl
Innerchr10:798721..820583hg19UCSC Ensembl
Outerchr10:798221..821083hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3821863
hg1921863
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622083
Supporting Variants
SamplesHG01589
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13664645
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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