A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624350



Internal ID6664517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99661984..99686782hg38UCSC Ensembl
Innerchr10:99661984..99686782hg38UCSC Ensembl
Outerchr10:99661484..99687282hg38UCSC Ensembl
chr10:101421741..101446539hg19UCSC Ensembl
Innerchr10:101421741..101446539hg19UCSC Ensembl
Outerchr10:101421241..101447039hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3824799
hg1924799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13912269
SamplesNA19238
Known GenesENTPD7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624350
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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