A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565516



Internal ID7036898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137498047..137502612hg38UCSC Ensembl
Outerchr9:140392499..140397064hg19UCSC Ensembl
Outerchr9:139512320..139516885hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382664
hg192664
hg182664
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992019
Supporting Variants
SamplesHuRef
Known GenesPNPLA7
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565516
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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