A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624371



Internal ID6664538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101232878..101240073hg38UCSC Ensembl
Innerchr10:101232878..101240073hg38UCSC Ensembl
Outerchr10:101232630..101240324hg38UCSC Ensembl
chr10:102992635..102999830hg19UCSC Ensembl
Innerchr10:102992635..102999830hg19UCSC Ensembl
Outerchr10:102992387..103000081hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg387196
hg197196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13913045, essv13913044
SamplesHG02374, HG02399
Known GenesLBX1-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624371
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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