A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623794



Internal ID7010650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72203033..72203990hg38UCSC Ensembl
Innerchr10:72203033..72203990hg38UCSC Ensembl
Outerchr10:72202761..72204314hg38UCSC Ensembl
chr10:73962791..73963748hg19UCSC Ensembl
Innerchr10:73962791..73963748hg19UCSC Ensembl
Outerchr10:73962519..73964072hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38958
hg19958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861583
SamplesHG00319
Known GenesASCC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623794
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