A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617007



Internal ID7003893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42298033..42300151hg38UCSC Ensembl
Innerchr8:42298033..42300151hg38UCSC Ensembl
Outerchr8:42297970..42300180hg38UCSC Ensembl
chr8:42155551..42157669hg19UCSC Ensembl
Innerchr8:42155551..42157669hg19UCSC Ensembl
Outerchr8:42155488..42157698hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg382119
hg192119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13183749
SamplesHG02076
Known GenesIKBKB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617007
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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