A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13415199



Internal ID5425958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19018569..19021948hg38UCSC Ensembl
Innerchr9:19018577..19021940hg38UCSC Ensembl
Outerchr9:19018561..19021956hg38UCSC Ensembl
chr9:19018567..19021946hg19UCSC Ensembl
Innerchr9:19018575..19021938hg19UCSC Ensembl
Outerchr9:19018559..19021954hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg383380
hg193380
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619889
Supporting Variants
SamplesNA18953
Known GenesFAM154A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13415199
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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