A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3888671



Internal ID11873200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113621714..113621796hg38UCSC Ensembl
chr6:113942916..113942998hg19UCSC Ensembl
chr6:114049609..114049691hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3883
hg1983
hg1883
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1495430
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3888671
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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