A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13695996



Internal ID4518028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11711951..11713289hg38UCSC Ensembl
Innerchr10:11711970..11713270hg38UCSC Ensembl
Outerchr10:11711932..11713308hg38UCSC Ensembl
chr10:11753950..11755288hg19UCSC Ensembl
Innerchr10:11753969..11755269hg19UCSC Ensembl
Outerchr10:11753931..11755307hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381339
hg191339
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622344
Supporting Variants
SamplesHG04018
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13695996
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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