A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13969373



Internal ID1770479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127492154..127497464hg38UCSC Ensembl
Innerchr10:127492170..127497449hg38UCSC Ensembl
Outerchr10:127492139..127497480hg38UCSC Ensembl
chr10:129290418..129295728hg19UCSC Ensembl
Innerchr10:129290434..129295713hg19UCSC Ensembl
Outerchr10:129290403..129295744hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg385311
hg195311
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624885
Supporting Variants
SamplesHG01626
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13969373
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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