A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13915189



Internal ID3917005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103971385..103974772hg38UCSC Ensembl
Innerchr10:103971450..103974707hg38UCSC Ensembl
Outerchr10:103971320..103974837hg38UCSC Ensembl
chr10:105731143..105734530hg19UCSC Ensembl
Innerchr10:105731208..105734465hg19UCSC Ensembl
Outerchr10:105731078..105734595hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg383388
hg193388
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624424
Supporting Variants
SamplesHG03914
Known GenesSLK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13915189
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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