A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13904802



Internal ID3080531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95485569..95494628hg38UCSC Ensembl
Innerchr10:95485569..95494628hg38UCSC Ensembl
Outerchr10:95485414..95494745hg38UCSC Ensembl
chr10:97245326..97254385hg19UCSC Ensembl
Innerchr10:97245326..97254385hg19UCSC Ensembl
Outerchr10:97245171..97254502hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg389060
hg199060
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624279
Supporting Variants
SamplesHG02702
Known GenesSORBS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13904802
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