A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624587



Internal ID6664751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112766318..112767228hg38UCSC Ensembl
Innerchr10:112766337..112767210hg38UCSC Ensembl
Outerchr10:112766300..112767247hg38UCSC Ensembl
chr10:114526077..114526987hg19UCSC Ensembl
Innerchr10:114526096..114526969hg19UCSC Ensembl
Outerchr10:114526059..114527006hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13939561, essv13939560
SamplesNA18966, HG03224
Known GenesVTI1A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624587
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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