A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13572615



Internal ID2749660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96594837..96605447hg38UCSC Ensembl
Innerchr9:96594837..96605447hg38UCSC Ensembl
Outerchr9:96594337..96605947hg38UCSC Ensembl
chr9:99357119..99367729hg19UCSC Ensembl
Innerchr9:99357119..99367729hg19UCSC Ensembl
Outerchr9:99356619..99368229hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3810611
hg1910611
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621166
Supporting Variants
SamplesHG02419
Known GenesCDC14B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13572615
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