A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13513837



Internal ID3080497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71145337..71150315hg38UCSC Ensembl
Innerchr9:71145337..71150315hg38UCSC Ensembl
Outerchr9:71145074..71150460hg38UCSC Ensembl
chr9:73760253..73765231hg19UCSC Ensembl
Innerchr9:73760253..73765231hg19UCSC Ensembl
Outerchr9:73759990..73765376hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg384979
hg194979
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620600
Supporting Variants
SamplesHG02702
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13513837
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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