A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13689361



Internal ID4827797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7718981..7721260hg38UCSC Ensembl
Innerchr10:7718981..7721260hg38UCSC Ensembl
Outerchr10:7718826..7721313hg38UCSC Ensembl
chr10:7760944..7763223hg19UCSC Ensembl
Innerchr10:7760944..7763223hg19UCSC Ensembl
Outerchr10:7760789..7763276hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382280
hg192280
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622276
Supporting Variants
SamplesNA12045
Known GenesITIH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13689361
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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