A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13744784



Internal ID3746600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29629598..29630068hg38UCSC Ensembl
Innerchr10:29629598..29630068hg38UCSC Ensembl
Outerchr10:29629598..29630068hg38UCSC Ensembl
chr10:29918527..29918997hg19UCSC Ensembl
Innerchr10:29918527..29918997hg19UCSC Ensembl
Outerchr10:29918527..29918997hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622777
Supporting Variants
SamplesHG00099
Known GenesSVIL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13744784
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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