A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3804836



Internal ID11610349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21981092..21981162hg38UCSC Ensembl
chr9:21981091..21981161hg19UCSC Ensembl
chr9:21971091..21971161hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3871
hg1971
hg1871
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1425040
Supporting Variants
SamplesHuRef
Known GenesCDKN2A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3804836
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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