A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3633770



Internal ID11781412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32778005..32778142hg38UCSC Ensembl
chr15:33070206..33070343hg19UCSC Ensembl
chr15:30857498..30857635hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38138
hg19138
hg18138
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1533512
Supporting Variants
SamplesHuRef
Known GenesFMN1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3633770
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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