A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13861599



Internal ID1317519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72475430..72496497hg38UCSC Ensembl
Innerchr10:72475930..72495997hg38UCSC Ensembl
Outerchr10:72474430..72497497hg38UCSC Ensembl
chr10:74235188..74256255hg19UCSC Ensembl
Innerchr10:74235688..74255755hg19UCSC Ensembl
Outerchr10:74234188..74257255hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3821068
hg1921068
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623797
Supporting Variants
SamplesHG01164
Known GenesMICU1, MIR1256
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13861599
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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