A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619473



Internal ID7006347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7867544..7870024hg38UCSC Ensembl
Innerchr9:7867574..7869994hg38UCSC Ensembl
Outerchr9:7867514..7870054hg38UCSC Ensembl
chr9:7867544..7870024hg19UCSC Ensembl
Innerchr9:7867574..7869994hg19UCSC Ensembl
Outerchr9:7867514..7870054hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg382481
hg192481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13394148
SamplesHG03941
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619473
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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