A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6001788



Internal ID9199312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132377277..132377397hg38UCSC Ensembl
Outerchr9:132377232..132377469hg38UCSC Ensembl
Innerchr9:135252664..135252784hg19UCSC Ensembl
Outerchr9:135252619..135252856hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678054
Supporting Variants
SamplesHG01515
Known GenesTTF1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6001788
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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