A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624124



Internal ID7010980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88340402..88343373hg38UCSC Ensembl
Innerchr10:88340404..88343371hg38UCSC Ensembl
Outerchr10:88340400..88343375hg38UCSC Ensembl
chr10:90100159..90103130hg19UCSC Ensembl
Innerchr10:90100161..90103128hg19UCSC Ensembl
Outerchr10:90100157..90103132hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg382972
hg192972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13889924, essv13889923, essv13889926, essv13889922, essv13889921, essv13889925
SamplesHG00149, HG02233, NA20536, HG01615, HG00141, NA19661
Known GenesRNLS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624124
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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