A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13559479



Internal ID1373795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92824715..92826453hg38UCSC Ensembl
Innerchr9:92824740..92826429hg38UCSC Ensembl
Outerchr9:92824691..92826478hg38UCSC Ensembl
chr9:95586997..95588735hg19UCSC Ensembl
Innerchr9:95587022..95588711hg19UCSC Ensembl
Outerchr9:95586973..95588760hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381739
hg191739
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621090
Supporting Variants
SamplesHG01242
Known GenesANKRD19P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13559479
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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