A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13945778



Internal ID3836972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116158976..116164023hg38UCSC Ensembl
Innerchr10:116158976..116164023hg38UCSC Ensembl
Outerchr10:116158753..116164222hg38UCSC Ensembl
chr10:117918488..117923535hg19UCSC Ensembl
Innerchr10:117918488..117923535hg19UCSC Ensembl
Outerchr10:117918265..117923734hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg385048
hg195048
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624650
Supporting Variants
SamplesHG03472
Known GenesGFRA1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13945778
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