A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3350808



Internal ID15197789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63333260..63342158hg38UCSC Ensembl
Innerchr9:63334260..63341158hg38UCSC Ensembl
Outerchr9:63332260..63343158hg38UCSC Ensembl
chr9:67288232..67297130hg19UCSC Ensembl
Innerchr9:67289232..67296130hg19UCSC Ensembl
Outerchr9:67287232..67298130hg19UCSC Ensembl
chr9:66978052..66986950hg18UCSC Ensembl
Innerchr9:66979052..66985950hg18UCSC Ensembl
Outerchr9:66977052..66987950hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg388899
hg198899
hg188899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697128
SamplesNA19240
Known GenesAQP7P1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3350808
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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