A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622095



Internal ID6662265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1018212..1031287hg38UCSC Ensembl
Innerchr10:1018362..1031137hg38UCSC Ensembl
Outerchr10:1018062..1031437hg38UCSC Ensembl
chr10:1064152..1077227hg19UCSC Ensembl
Innerchr10:1064302..1077077hg19UCSC Ensembl
Outerchr10:1064002..1077377hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3813076
hg1913076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13664670
SamplesHG00109
Known GenesIDI2, IDI2-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622095
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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