A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13411605



Internal ID1854563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17095699..17100732hg38UCSC Ensembl
Innerchr9:17095703..17100728hg38UCSC Ensembl
Outerchr9:17095695..17100736hg38UCSC Ensembl
chr9:17095697..17100730hg19UCSC Ensembl
Innerchr9:17095701..17100726hg19UCSC Ensembl
Outerchr9:17095693..17100734hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg385034
hg195034
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619832
Supporting Variants
SamplesHG01756
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13411605
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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