A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620934



Internal ID7007804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85289730..85298122hg38UCSC Ensembl
Innerchr9:85290230..85297622hg38UCSC Ensembl
Outerchr9:85288730..85299122hg38UCSC Ensembl
chr9:87904645..87913037hg19UCSC Ensembl
Innerchr9:87905145..87912537hg19UCSC Ensembl
Outerchr9:87903645..87914037hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg388393
hg198393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13543284
SamplesHG03558
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620934
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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