A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4223659



Internal ID11506197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2605292..2605352hg38UCSC Ensembl
chr6:2605526..2605586hg19UCSC Ensembl
chr6:2550525..2550585hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3861
hg1961
hg1861
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1107487
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4223659
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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