A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623180



Internal ID6663348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49888587..49900297hg38UCSC Ensembl
Innerchr10:49888655..49900229hg38UCSC Ensembl
Outerchr10:49888519..49900365hg38UCSC Ensembl
chr10:51096633..51108343hg19UCSC Ensembl
Innerchr10:51096701..51108275hg19UCSC Ensembl
Outerchr10:51096565..51108411hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3811711
hg1911711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13797150
SamplesHG01686
Known GenesPARG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623180
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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