A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620590



Internal ID7007460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71032985..71060193hg38UCSC Ensembl
Innerchr9:71032985..71060193hg38UCSC Ensembl
Outerchr9:71032485..71060693hg38UCSC Ensembl
chr9:73647901..73675109hg19UCSC Ensembl
Innerchr9:73647901..73675109hg19UCSC Ensembl
Outerchr9:73647401..73675609hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3827209
hg1927209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13513335
SamplesHG04023
Known GenesTRPM3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620590
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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