A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4106042



Internal ID11655833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95195517..95196488hg38UCSC Ensembl
chr2:95861265..95862236hg19UCSC Ensembl
chr2:95224992..95225963hg18UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38972
hg19972
hg18972
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1774443
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4106042
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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