A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13752227



Internal ID3754043
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622893
Supporting Variants
SamplesHG03640
Known GenesCREM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13752227
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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