A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3613629



Internal ID11801553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50445310..50445616hg38UCSC Ensembl
chr15:50737507..50737813hg19UCSC Ensembl
chr15:48524799..48525105hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38307
hg19307
hg18307
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1049679
Supporting Variants
SamplesHuRef
Known GenesUSP8
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3613629
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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