A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13572586



Internal ID1900568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96410090..96411831hg38UCSC Ensembl
Innerchr9:96410093..96411828hg38UCSC Ensembl
Outerchr9:96410087..96411834hg38UCSC Ensembl
chr9:99172372..99174113hg19UCSC Ensembl
Innerchr9:99172375..99174110hg19UCSC Ensembl
Outerchr9:99172369..99174116hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381742
hg191742
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621164
Supporting Variants
SamplesHG01784
Known GenesZNF367
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13572586
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