A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13449246



Internal ID1813268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32318465..32325890hg38UCSC Ensembl
Innerchr9:32318482..32325874hg38UCSC Ensembl
Outerchr9:32318449..32325907hg38UCSC Ensembl
chr9:32318463..32325888hg19UCSC Ensembl
Innerchr9:32318480..32325872hg19UCSC Ensembl
Outerchr9:32318447..32325905hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg387426
hg197426
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620294
Supporting Variants
SamplesHG01685
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13449246
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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