A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13508341



Internal ID3510157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69189604..69190081hg38UCSC Ensembl
Innerchr9:69189604..69190081hg38UCSC Ensembl
Outerchr9:69189604..69190081hg38UCSC Ensembl
chr9:71804520..71804997hg19UCSC Ensembl
Innerchr9:71804520..71804997hg19UCSC Ensembl
Outerchr9:71804520..71804997hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620554
Supporting Variants
SamplesNA11829
Known GenesTJP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13508341
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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