A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621193



Internal ID6661372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97596188..97658370hg38UCSC Ensembl
Innerchr9:97596338..97658220hg38UCSC Ensembl
Outerchr9:97596038..97658520hg38UCSC Ensembl
chr9:100358470..100420652hg19UCSC Ensembl
Innerchr9:100358620..100420502hg19UCSC Ensembl
Outerchr9:100358320..100420802hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3862183
hg1962183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1494e214
Supporting Variantsessv13573737, essv13573736
SamplesHG01602, HG04152
Known GenesNCBP1, TMOD1, TSTD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621193
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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