A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3825900



Internal ID11589285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29420487..29420828hg38UCSC Ensembl
chr12:29573420..29573761hg19UCSC Ensembl
chr12:29464687..29465028hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38342
hg19342
hg18342
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1371683
Supporting Variants
SamplesHuRef
Known GenesOVCH1-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3825900
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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