A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13378535



Internal ID3257000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1723969..1770519hg38UCSC Ensembl
Innerchr9:1723969..1770519hg38UCSC Ensembl
Outerchr9:1723469..1771019hg38UCSC Ensembl
chr9:1723969..1770519hg19UCSC Ensembl
Innerchr9:1723969..1770519hg19UCSC Ensembl
Outerchr9:1723469..1771019hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3846551
hg1946551
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619276
Supporting Variants
SamplesHG02879
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13378535
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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