A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3775092



Internal ID11986779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30601463..30601798hg38UCSC Ensembl
chr13:31175600..31175935hg19UCSC Ensembl
chr13:30073600..30073935hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38336
hg19336
hg18336
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1720901
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3775092
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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