A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3887450



Internal ID11527735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3694335..3694755hg38UCSC Ensembl
chr1:3610899..3611319hg19UCSC Ensembl
chr1:3600759..3601179hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38421
hg19421
hg18421
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1634361
Supporting Variants
SamplesHuRef
Known GenesTP73
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3887450
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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