A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623797



Internal ID7010653
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861599
SamplesHG01164
Known GenesMICU1, MIR1256
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623797
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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