A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3956944



Internal ID11458242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131680928..131681092hg38UCSC Ensembl
chr11:131550822..131550986hg19UCSC Ensembl
chr11:131056032..131056196hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38165
hg19165
hg18165
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1453063
Supporting Variants
SamplesHuRef
Known GenesNTM
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3956944
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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