A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3656912



Internal ID11758271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24811659..24817734hg38UCSC Ensembl
chr6:24811887..24817962hg19UCSC Ensembl
chr6:24919866..24925941hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg386076
hg196076
hg186076
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1071217
Supporting Variants
SamplesHuRef
Known GenesFAM65B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3656912
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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