A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13462178



Internal ID941344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36474160..36475002hg38UCSC Ensembl
Innerchr9:36474203..36474960hg38UCSC Ensembl
Outerchr9:36474118..36475045hg38UCSC Ensembl
chr9:36474157..36474999hg19UCSC Ensembl
Innerchr9:36474200..36474957hg19UCSC Ensembl
Outerchr9:36474115..36475042hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620396
Supporting Variants
SamplesHG00565
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13462178
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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