A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13606212



Internal ID3608029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112434839..112437731hg38UCSC Ensembl
Innerchr9:112434839..112437731hg38UCSC Ensembl
Outerchr9:112434403..112437972hg38UCSC Ensembl
chr9:115197119..115200011hg19UCSC Ensembl
Innerchr9:115197119..115200011hg19UCSC Ensembl
Outerchr9:115196683..115200252hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382893
hg192893
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621515
Supporting Variants
SamplesHG03436
Known GenesHSDL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13606212
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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