A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13969374



Internal ID2919244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127520664..127522790hg38UCSC Ensembl
Innerchr10:127520682..127522772hg38UCSC Ensembl
Outerchr10:127520646..127522808hg38UCSC Ensembl
chr10:129318928..129321054hg19UCSC Ensembl
Innerchr10:129318946..129321036hg19UCSC Ensembl
Outerchr10:129318910..129321072hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382127
hg192127
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624886
Supporting Variants
SamplesHG02583
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13969374
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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