A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622893



Internal ID6663062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35161367..35165012hg38UCSC Ensembl
Innerchr10:35161395..35164985hg38UCSC Ensembl
Outerchr10:35161340..35165040hg38UCSC Ensembl
chr10:35450295..35453940hg19UCSC Ensembl
Innerchr10:35450323..35453913hg19UCSC Ensembl
Outerchr10:35450268..35453968hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg383646
hg193646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13752228, essv13752227
SamplesHG03663, HG03640
Known GenesCREM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622893
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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