A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623983



Internal ID7010839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:81876350..81877417hg38UCSC Ensembl
Innerchr10:81876376..81877391hg38UCSC Ensembl
Outerchr10:81876324..81877443hg38UCSC Ensembl
chr10:83636106..83637173hg19UCSC Ensembl
Innerchr10:83636132..83637147hg19UCSC Ensembl
Outerchr10:83636080..83637199hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381068
hg191068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13875562, essv13875561, essv13875563
SamplesNA19443, NA18536, HG00446
Known GenesNRG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623983
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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