A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623162



Internal ID6663330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49011836..49038527hg38UCSC Ensembl
Innerchr10:49011889..49038474hg38UCSC Ensembl
Outerchr10:49011783..49038580hg38UCSC Ensembl
chr10:50219881..50246572hg19UCSC Ensembl
Innerchr10:50219934..50246519hg19UCSC Ensembl
Outerchr10:50219828..50246625hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3826692
hg1926692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13796114
SamplesHG00115
Known GenesVSTM4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623162
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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