A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620365



Internal ID7007236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34935418..34938753hg38UCSC Ensembl
Innerchr9:34935477..34938695hg38UCSC Ensembl
Outerchr9:34935360..34938812hg38UCSC Ensembl
chr9:34935415..34938750hg19UCSC Ensembl
Innerchr9:34935474..34938692hg19UCSC Ensembl
Outerchr9:34935357..34938809hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383336
hg193336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13459061, essv13459060, essv13459062
SamplesNA19443, NA18962, HG00463
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620365
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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