A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4313901



Internal ID11596439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28926942..28927561hg38UCSC Ensembl
chr6:28894719..28895338hg19UCSC Ensembl
chr6:29002698..29003317hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38620
hg19620
hg18620
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1445670
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4313901
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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