A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13559429



Internal ID3561245
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621079
Supporting Variants
SamplesHG03028
Known GenesCENPP, OMD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13559429
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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