A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13415197



Internal ID3241431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18975002..18994758hg38UCSC Ensembl
Innerchr9:18975002..18994758hg38UCSC Ensembl
Outerchr9:18974502..18995258hg38UCSC Ensembl
chr9:18975000..18994756hg19UCSC Ensembl
Innerchr9:18975000..18994756hg19UCSC Ensembl
Outerchr9:18974500..18995256hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3819757
hg1919757
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619888
Supporting Variants
SamplesHG02855
Known GenesFAM154A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13415197
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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