A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624167



Internal ID7011023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89809570..89946268hg38UCSC Ensembl
Innerchr10:89809570..89946268hg38UCSC Ensembl
Outerchr10:89809070..89946768hg38UCSC Ensembl
chr10:91569327..91706025hg19UCSC Ensembl
Innerchr10:91569327..91706025hg19UCSC Ensembl
Outerchr10:91568827..91706525hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38136699
hg19136699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13890849
SamplesHG03950
Known GenesLINC00865
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624167
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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