A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13552296



Internal ID1728131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90010595..90168622hg38UCSC Ensembl
Innerchr9:90010745..90168472hg38UCSC Ensembl
Outerchr9:90010445..90168772hg38UCSC Ensembl
chr9:92772877..92930904hg19UCSC Ensembl
Innerchr9:92773027..92930754hg19UCSC Ensembl
Outerchr9:92772727..92931054hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38158028
hg19158028
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621038
Supporting Variants
SamplesHG01602
Known GenesLOC286370, MIR4290
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13552296
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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