A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161562



Internal ID7906276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73598645..74203212hg38UCSC Ensembl
Innerchr9:76213561..76818128hg19UCSC Ensembl
Innerchr9:75403381..76007948hg18UCSC Ensembl
Innerchr9:73443115..74047682hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38604568
hg19604568
hg18604568
hg17604568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422439
Supporting Variants
SamplesND01938
Known GenesMIR6130
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161562
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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