A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3632112



Internal ID12129756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134133211..134134148hg38UCSC Ensembl
chr9:136998333..136999270hg19UCSC Ensembl
chr9:135988154..135989091hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38938
hg19938
hg18938
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1261185
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3632112
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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