A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624847



Internal ID7011697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125946804..125963970hg38UCSC Ensembl
Innerchr10:125946804..125963970hg38UCSC Ensembl
Outerchr10:125946304..125964470hg38UCSC Ensembl
chr10:127635373..127652539hg19UCSC Ensembl
Innerchr10:127635373..127652539hg19UCSC Ensembl
Outerchr10:127634873..127653039hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3817167
hg1917167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13964373
SamplesHG02675
Known GenesFANK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624847
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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