A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13648200



Internal ID2358585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135000411..135009519hg38UCSC Ensembl
Innerchr9:135000411..135009519hg38UCSC Ensembl
Outerchr9:134999911..135010019hg38UCSC Ensembl
chr9:137892257..137901365hg19UCSC Ensembl
Innerchr9:137892257..137901365hg19UCSC Ensembl
Outerchr9:137891757..137901865hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg389109
hg199109
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621973
Supporting Variants
SamplesHG02088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13648200
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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