A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621079



Internal ID6661260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92419331..92422195hg38UCSC Ensembl
Innerchr9:92419368..92422159hg38UCSC Ensembl
Outerchr9:92419295..92422232hg38UCSC Ensembl
chr9:95181613..95184477hg19UCSC Ensembl
Innerchr9:95181650..95184441hg19UCSC Ensembl
Outerchr9:95181577..95184514hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382865
hg192865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559429
SamplesHG03028
Known GenesCENPP, OMD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621079
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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