A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13538750



Internal ID3337796
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620881
Supporting Variants
SamplesHG02977
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13538750
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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