A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622427



Internal ID6662597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14605891..14606814hg38UCSC Ensembl
Innerchr10:14605924..14606781hg38UCSC Ensembl
Outerchr10:14605858..14606847hg38UCSC Ensembl
chr10:14647890..14648813hg19UCSC Ensembl
Innerchr10:14647923..14648780hg19UCSC Ensembl
Outerchr10:14647857..14648846hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38924
hg19924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13704029
SamplesHG00640
Known GenesFAM107B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622427
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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