A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624926



Internal ID7011776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130055768..130103309hg38UCSC Ensembl
Innerchr10:130055809..130103268hg38UCSC Ensembl
Outerchr10:130055727..130103350hg38UCSC Ensembl
chr10:131854032..131901573hg19UCSC Ensembl
Innerchr10:131854073..131901532hg19UCSC Ensembl
Outerchr10:131853991..131901614hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3847542
hg1947542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13974701
SamplesHG00345
Known GenesLINC00959
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624926
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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