A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13383924



Internal ID2139368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4900039..4901474hg38UCSC Ensembl
Innerchr9:4900062..4901451hg38UCSC Ensembl
Outerchr9:4900016..4901497hg38UCSC Ensembl
chr9:4900039..4901474hg19UCSC Ensembl
Innerchr9:4900062..4901451hg19UCSC Ensembl
Outerchr9:4900016..4901497hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381436
hg191436
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619361
Supporting Variants
SamplesHG01939
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13383924
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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