A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621906



Internal ID7008772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131990552..131993794hg38UCSC Ensembl
Innerchr9:131990702..131993644hg38UCSC Ensembl
Outerchr9:131990402..131993944hg38UCSC Ensembl
chr9:134865939..134869181hg19UCSC Ensembl
Innerchr9:134866089..134869031hg19UCSC Ensembl
Outerchr9:134865789..134869331hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg383243
hg193243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13633397
SamplesHG02151
Known GenesMED27
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621906
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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