A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620415



Internal ID7007286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38035658..38039487hg38UCSC Ensembl
Innerchr9:38035658..38039487hg38UCSC Ensembl
Outerchr9:38035527..38039605hg38UCSC Ensembl
chr9:38035655..38039484hg19UCSC Ensembl
Innerchr9:38035655..38039484hg19UCSC Ensembl
Outerchr9:38035524..38039602hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg383830
hg193830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13464433
SamplesNA19436
Known GenesSHB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620415
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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