A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13505790



Internal ID3507606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69123203..69128443hg38UCSC Ensembl
Innerchr9:69123203..69128443hg38UCSC Ensembl
Outerchr9:69123203..69128443hg38UCSC Ensembl
chr9:71738119..71743359hg19UCSC Ensembl
Innerchr9:71738119..71743359hg19UCSC Ensembl
Outerchr9:71738119..71743359hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385241
hg195241
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620552
Supporting Variants
SamplesHG02090
Known GenesTJP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13505790
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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