A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13946486



Internal ID5426302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117394730..117395658hg38UCSC Ensembl
Innerchr10:117394747..117395641hg38UCSC Ensembl
Outerchr10:117394713..117395675hg38UCSC Ensembl
chr10:119154241..119155169hg19UCSC Ensembl
Innerchr10:119154258..119155152hg19UCSC Ensembl
Outerchr10:119154224..119155186hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624678
Supporting Variants
SamplesNA18953
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13946486
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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