A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621786



Internal ID7008652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127597138..127600610hg38UCSC Ensembl
Innerchr9:127597288..127600460hg38UCSC Ensembl
Outerchr9:127596988..127600760hg38UCSC Ensembl
chr9:130359417..130362889hg19UCSC Ensembl
Innerchr9:130359567..130362739hg19UCSC Ensembl
Outerchr9:130359267..130363039hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383473
hg193473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13622623, essv13622621, essv13622620, essv13622619, essv13622622
SamplesHG00729, NA19917, HG02152, HG02379, HG02353
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621786
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer