A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13704034



Internal ID3705850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14755268..14758895hg38UCSC Ensembl
Innerchr10:14755330..14758834hg38UCSC Ensembl
Outerchr10:14755207..14758957hg38UCSC Ensembl
chr10:14797267..14800894hg19UCSC Ensembl
Innerchr10:14797329..14800833hg19UCSC Ensembl
Outerchr10:14797206..14800956hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383628
hg193628
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622429
Supporting Variants
SamplesHG00543
Known GenesFAM107B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13704034
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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