A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624668



Internal ID7011519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116954585..116956680hg38UCSC Ensembl
Innerchr10:116954605..116956661hg38UCSC Ensembl
Outerchr10:116954566..116956700hg38UCSC Ensembl
chr10:118714096..118716191hg19UCSC Ensembl
Innerchr10:118714116..118716172hg19UCSC Ensembl
Outerchr10:118714077..118716211hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg382096
hg192096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13946437
SamplesNA19085
Known GenesKIAA1598
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624668
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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