A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13890520



Internal ID3892336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88958203..88963844hg38UCSC Ensembl
Innerchr10:88958353..88963694hg38UCSC Ensembl
Outerchr10:88958053..88963994hg38UCSC Ensembl
chr10:90717960..90723601hg19UCSC Ensembl
Innerchr10:90718110..90723451hg19UCSC Ensembl
Outerchr10:90717810..90723751hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg385642
hg195642
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624145
Supporting Variants
SamplesHG03419
Known GenesACTA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13890520
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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