A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3900276



Internal ID11861595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39360051..39361349hg38UCSC Ensembl
chr13:39934188..39935486hg19UCSC Ensembl
chr13:38832188..38833486hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1412441
Supporting Variants
SamplesHuRef
Known GenesLHFP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3900276
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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