A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13664658



Internal ID6362419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:941255..955284hg38UCSC Ensembl
Innerchr10:941255..955284hg38UCSC Ensembl
Outerchr10:940755..955784hg38UCSC Ensembl
chr10:987195..1001224hg19UCSC Ensembl
Innerchr10:987195..1001224hg19UCSC Ensembl
Outerchr10:986695..1001724hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3814030
hg1914030
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622090
Supporting Variants
SamplesNA20294
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13664658
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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