A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621082



Internal ID6661263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92558897..92575329hg38UCSC Ensembl
Innerchr9:92558909..92575317hg38UCSC Ensembl
Outerchr9:92558885..92575341hg38UCSC Ensembl
chr9:95321179..95337611hg19UCSC Ensembl
Innerchr9:95321191..95337599hg19UCSC Ensembl
Outerchr9:95321167..95337623hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3816433
hg1916433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559434, essv13559433, essv13559435
SamplesHG00851, NA20507, HG02820
Known GenesCENPP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621082
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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