A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13770353



Internal ID3750254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45530615..45550937hg38UCSC Ensembl
Innerchr10:45530615..45550937hg38UCSC Ensembl
Outerchr10:45530115..45551437hg38UCSC Ensembl
chr10:46026063..46046385hg19UCSC Ensembl
Innerchr10:46026063..46046385hg19UCSC Ensembl
Outerchr10:46025563..46046885hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3820323
hg1920323
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623097
Supporting Variants
SamplesHG03380
Known GenesMARCH8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13770353
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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