A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13899552



Internal ID2288443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93282005..93285994hg38UCSC Ensembl
Innerchr10:93282021..93285978hg38UCSC Ensembl
Outerchr10:93281989..93286010hg38UCSC Ensembl
chr10:95041762..95045751hg19UCSC Ensembl
Innerchr10:95041778..95045735hg19UCSC Ensembl
Outerchr10:95041746..95045767hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg383990
hg193990
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624237
Supporting Variants
SamplesHG02048
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13899552
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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