A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624320



Internal ID7011176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97683821..97684700hg38UCSC Ensembl
Innerchr10:97683821..97684700hg38UCSC Ensembl
Outerchr10:97683608..97684925hg38UCSC Ensembl
chr10:99443578..99444457hg19UCSC Ensembl
Innerchr10:99443578..99444457hg19UCSC Ensembl
Outerchr10:99443365..99444682hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13908837, essv13908838, essv13908840, essv13908841, essv13908839
SamplesHG01242, NA19404, NA19317, NA19449, NA19468
Known GenesAVPI1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624320
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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