A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622268



Internal ID7009127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7260096..7367838hg38UCSC Ensembl
Innerchr10:7260103..7367831hg38UCSC Ensembl
Outerchr10:7260089..7367845hg38UCSC Ensembl
chr10:7302058..7409800hg19UCSC Ensembl
Innerchr10:7302065..7409793hg19UCSC Ensembl
Outerchr10:7302051..7409807hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38107743
hg19107743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13689286
SamplesHG02561
Known GenesSFMBT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622268
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer