A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13419720



Internal ID1467067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21650013..21655792hg38UCSC Ensembl
Innerchr9:21650013..21655792hg38UCSC Ensembl
Outerchr9:21649788..21655997hg38UCSC Ensembl
chr9:21650012..21655791hg19UCSC Ensembl
Innerchr9:21650012..21655791hg19UCSC Ensembl
Outerchr9:21649787..21655996hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg385780
hg195780
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619966
Supporting Variants
SamplesHG01354
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13419720
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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