A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13657216



Internal ID680696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136735001..136751056hg38UCSC Ensembl
Innerchr9:136735034..136751024hg38UCSC Ensembl
Outerchr9:136734969..136751089hg38UCSC Ensembl
chr9:139629453..139645508hg19UCSC Ensembl
Innerchr9:139629486..139645476hg19UCSC Ensembl
Outerchr9:139629421..139645541hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3816056
hg1916056
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622013
Supporting Variants
SamplesHG00319
Known GenesLCN10, LCN6, LOC100128593, MIR6722
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13657216
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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