A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13913384



Internal ID2936339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101634254..101635335hg38UCSC Ensembl
Innerchr10:101634255..101635335hg38UCSC Ensembl
Outerchr10:101634254..101635336hg38UCSC Ensembl
chr10:103394011..103395092hg19UCSC Ensembl
Innerchr10:103394012..103395092hg19UCSC Ensembl
Outerchr10:103394011..103395093hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624386
Supporting Variants
SamplesHG02595
Known GenesFBXW4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13913384
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