A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620881



Internal ID7007751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82042217..82048072hg38UCSC Ensembl
Innerchr9:82042232..82048058hg38UCSC Ensembl
Outerchr9:82042203..82048087hg38UCSC Ensembl
chr9:84657132..84662987hg19UCSC Ensembl
Innerchr9:84657147..84662973hg19UCSC Ensembl
Outerchr9:84657118..84663002hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg385856
hg195856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13538751, essv13538750
SamplesHG03572, HG02977
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620881
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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